NEW METHYLENEBISPHENYL COMPOUNDS USEFUL IN THE TREATMENT OF INFLAMMATION

Field of the Invention

This invention relates to novel pharmaceutically-useful compounds, which compounds are useful as inhibitors of the production of leukotrienes, such as leukotriene C ₄ . The compounds are of potential utility in the treatment of respiratory and/or inflammatory diseases. The invention also relates to the use of such compounds as medicaments, to pharmaceutical compositions containing them, and to synthetic routes for their production.

Background of the Invention

Arachidonic acid is a fatty acid that is essential in the body and is stored in cell membranes. It may be converted, e.g. in the event of inflammation, into mediators, some of which are known to have beneficial properties and others that are harmful. Such mediators include leukotrienes (formed by the action of 5-lipoxygenase (5-LO), which acts by catalysing the insertion of molecular oxygen into carbon position 5) and prostaglandins (which are formed by the action of cyclooxygenases (COXs)). Huge efforts have been devoted towards the development of drugs that inhibit the action of these metabolites as well as the biological processes that form them.

Of the leukotrienes, leukotriene (LT) B ₄ is known to be a strong proinflammatory mediator, while the cysteinyl-containing leukotrienes C ₄ , D ₄ and E ₄ (CysLTs) are mainly very potent bronchoconstrictors and have thus been implicated in the pathobiology of asthma. It has also been suggested that the CysLTs play a role in inflammatory mechanisms. The biological activities of the CysLTs are mediated through two receptors designated CySLT ₁ and CysLT ₂ , but the existence of additional CysLT receptors has also been proposed. Leukotriene receptor antagonists (LTRAs) have been developed for the treatment of asthma, but they are often highly selective for CysLTi. It may be hypothesised that better control of asthma, and possibly also COPD, may be attained if the activity of both of the CysLT receptors could be reduced. This may be achieved by developing unselective LTRAs, but also by inhibiting the activity of proteins, e.g. enzymes,

involved in the synthesis of the CysLTs; 5-LO, 5-lipoxygenase-activating protein (FLAP), and leukotriene C ₄ synthase may be mentioned. However, a 5-LO or a FLAP inhibitor would also decrease the formation of LTB ₄ . For a review on leukotrienes in asthma, see H. -E Claesson and S. -E. Dahlen J. Internal Med. 245, 205 (1999).

There are many diseases/disorders that are inflammatory in their nature or have an inflammatory component. One of the major problems associated with existing treatments of inflammatory conditions is a lack of efficacy and/or the prevalence of side effects (real or perceived).

Asthma is a chronic inflammatory disease affecting 6% to 8% of the adult population of the industrialized world. In children, the incidence is even higher, being close to 10% in most countries. Asthma is the most common cause of hospitalization for children under the age of fifteen.

Treatment regimens for asthma are based on the severity of the condition. Mild cases are either untreated or are only treated with inhaled β-agonists. Patients with more severe asthma are typically treated with anti-inflammatory compounds on a regular basis.

There is a considerable under-treatment of asthma, which is due at least in part to perceived risks with existing maintenance therapy (mainly inhaled corticosteroids). These include risks of growth retardation in children and loss of bone mineral density, resulting in unnecessary morbidity and mortality. As an alternative to steroids, LTRAs have been developed. These drugs may be given orally, but are considerably less efficacious than inhaled steroids and usually do not control airway inflammation satisfactorily.

This combination of factors has led to at least 50% of all asthma patients being inadequately treated.

A similar pattern of under-treatment exists in relation to allergic disorders, where drugs are available to treat a number of common conditions but are underused in view of apparent side effects. Rhinitis, conjunctivitis and dermatitis may have an

allergic component, but may also arise in the absence of underlying allergy. Indeed, non-allergic conditions of this class are in many cases more difficult to treat.

Chronic obstructive pulmonary disease (COPD) is a common disease affecting 6% to 8% of the world population. The disease is potentially lethal, and the morbidity and mortality from the condition is considerable. At present, there is no known pharmacological treatment capable of changing the course of COPD.

Other inflammatory disorders which may be mentioned include:

(a) pulmonary fibrosis (this is less common than COPD, but is a serious disorder with a very bad prognosis. No curative treatment exists);

(b) inflammatory bowel disease (a group of disorders with a high morbidity rate. Today only symptomatic treatment of such disorders is available); and

(c) rheumatoid arthritis and osteoarthritis (common disabling inflammatory disorders of the joints. There are currently no curative, and only moderately effective symptomatic, treatments available for the management of such conditions).

Inflammation is also a common cause of pain. Inflammatory pain may arise for numerous reasons, such as infection, surgery or other trauma. Moreover, several malignancies are known to have inflammatory components adding to the symptomatology of the patients.

Thus, new and/or alternative treatments for respiratory and/or inflammatory disorders would be of benefit to all of the above-mentioned patient groups. In particular, there is a real and substantial unmet clinical need for an effective antiinflammatory drug capable of treating inflammatory disorders, in particular asthma and COPD, with no real or perceived side effects.

The listing or discussion of an apparently prior-published document in this specification should not necessarily be taken as an acknowledgement that the document is part of the state of the art or is common general knowledge.

Internationa! patent application WO 2005/092836 discloses various biaryl compounds. However, such compounds are only described as being useful opioid receptor antagonists, and therefore useful in the treatment of obesity and related diseases such as diabetes.

International patent application WO 2007/113337 discloses various biaryl sulfonamides. However, such compounds are only described as being useful fluorescent markers of proteins, for use in high throughput screening tests.

International patent application WO 2005/083081 discloses a biaryl sulphonamide that is useful as a nuclease inhibitor.

International patent application WO 2004/076640 discloses a biaryl sulfonamide compound that is useful as an inhibitor of angiogenin and RNases.

Kao, R. Y. T., et a/., P. Natl. Acad. ScL USA, 2002, 99(15), 10066-10071 and Jenkins, J. L., Protein, 2003, 50, 81-93 both disclose various biaryl sulfonamides as angiogenin inhibitors.

US patents Nos. US 2,438,782 and US 2,435,629 and UK patent No. GB 577,387 all disclose biaryl sulfonamides useful as, or in the synthesis of, photographic dyes.

Finally, Li, J. et al., Bioorg. Med. Chem., 2006, 14, 2209-2224 discloses various biaryl compounds that are purportedly useful as inhibitors of human cyclophilin A.

There is no disclosure in any of the prior art of derivatives of 5,5 ^' -methylenebis(2- aminobenzoic acid) for use as LTC ₄ synthase inhibitors, and therefore for use in the treatment of inflammation or respiratory disorders.

Disclosure of the Invention

According to the invention, there is provided a compound of formula I,

wherein

Y ¹ represents H or -Ar ¹ ; Y ² represents H or -Ar ² ; provided that at least one of Y ¹ and Y ² is other than H;

X ¹ and X ² independently represent one or more optional substituents selected from halo, -R ^3a , -CN, -C(O)R ^3b , -C(O)OR ³⁰ , -C(O)N(R ^4a )R ^5a , -N(R ^4b )R ^5b , -N(R ^3d )C(O)R ^4c , -N(R ³⁶ JC(O)N(R^)R ⁵ ", -N(R ^3f )C(O)OR ^4e , -N ₃ , -NO ₂ , -N(R ^3g )S(O) ₂ N(R ^4f )R ^5f , -OR ^3h , -OC(O)N(R ^4g )R ^5g , -OS(O) ₂ R ³¹ , -S(O) _m R ^3j , -N(R ^3k )S(O) ₂ R ^3m , -OC(O)R ³ⁿ , -OC(O)OR ^3p , -S(O) ₂ N(R ^4h )R ^5h and -OS(O) ₂ N(R ⁴ⁱ )R ⁵ⁱ ;

m represents 0, 1 or 2;

R ^3b to R ^3h , R ^3j , R ^3k , R ^3π , R ^4a to R ⁴ⁱ , R ^5a , R ^5b , R ^5d and R ^5f to R ⁵ⁱ independently represent H or R ^3a ; or any of the pairs R ⁴³ and R ^5a , R ^4b and R ^5b , R ^4d and R ^5d , R ^4f and R ^5f , R ⁴⁹ and R ^5g , R ^4h and R ^5h or R ⁴ⁱ and R ⁵ⁱ may be linked together to form a 3- to 6-membered ring, which ring optionally contains a further heteroatom (such as nitrogen or oxygen) in addition to the nitrogen atom to which these substituents are necessarily attached, and which ring is optionally substituted by F, Cl, =0 or R ^3a ;

R ³ⁱ , R ^3m and R ^3p independently represent R ^3a ;

R represents, on each occasion when mentioned above, d- ₆ alkyl optionally substituted by one or more substituents selected from F, Cl, -CN ₁ -N ₃ , =0, -OR ^6a , -N(R ^6b )R ^7b , -S(0) _n R ^6c , -S(O) ₂ N(R ^6d )R ^7d or -OS(O) ₂ N(R ^6e )R ^7e ;

n represents 0, 1 or 2;

R ^6a , R ^6b , R ^6c , R ^6d and R ^6e independently represent H or C _L6 alkyl optionally substituted by one or more substituents selected from F, Cl, =0, -OR ^8a , -N(R ^9a )R ^1Oa or -S(O) ₂ -M ¹ ;

R ^7b , R ^7d and R ^7e independently represent H, -S(O) ₂ CH ₃ , -S(O) ₂ CF ₃ or C _1-6 alkyl optionally substituted by one or more substituents selected from F, Cl, =0, -0R ^11a , -N(R ^12a )R ^13a or -S(O) ₂ -M ² ; or R ^6b and R ^7b , R ^6d and R ^7d or R ^6e and R ^7e may be linked together to form a 3- to 6- membered ring, which ring optionally contains a further heteroatom (such as nitrogen or oxygen) in addition to the nitrogen atom to which these substituents are necessarily attached, and which ring is optionally substituted by F, Cl, =0 or Ci _-3 alkyl optionally substituted by one or more substituents selected from =0 and fluoro;

M ¹ and M ² independently represent -CH ₃ , -CH ₂ CH ₃ , -CF ₃ or -N(R ^14a )R ^15a ;

R ^Ba and R ^11a independently represent H, -CH ₃ , -CH ₂ CH ₃ , -CF ₃ or -CHF ₂ ;

R ^9a , R ^1Oa , R ^12a , R ^13a , R ^14a and R ^15a independently represent H, -CH ₃ or -CH ₂ CH ₃ ,

Ar ¹ and Ar ² independently represent an aryl group or a heteroaryl group, both of which groups are optionally substituted by one or more substituents selected from A;

A represents, on each occasion when mentioned above:

I) an aryl group or a heteroaryl group, both of which are optionally substituted by one or more substituents selected from B; II) Ci _-8 alkyl or a heterocycloalkyl group, both of which are optionally substituted by one or more substituents selected from G ¹ and/or Z ¹ ; or III) a G ¹ group;

G ¹ represents, on each occasion when mentioned above, halo, cyano, -N ₃ , -NO ₂ , -ONO ₂ or -A ¹ -R ^16a ;

wherein A ¹ represents a single bond or a spacer group selected from -C(O)A ² -, -S-, -S(O) ₂ A ³ -, -N(R ^17a )A ⁴ - or -OA ⁵ -, in which: A ² represents a single bond, -O-, -N(R ^17b )- or -C(O)-; A ³ represents a single bond, -O- or -N(R ^17c )-; A ⁴ and A ⁵ independently represent a single bond, -C(O)-, -C(O)N(R ¹⁷ ")-, -C(O)O-, -S(O) ₂ - or -S(O) ₂ N(R ¹⁷⁶ )-;

Z ¹ represents, on each occasion when mentioned above, =0, =S, =N0R ^16b , =NS(O) ₂ N(R ^17f )R ^16c , =NCN or =C(H)NO ₂ ;

B represents, on each occasion when mentioned above:

I) an aryl group or a heteroaryl group, both of which are optionally substituted by one or more substituents selected from G ² ;

II) C _1-8 alkyl or a heterocycloalkyl group, both of which are optionally substituted by one or more substituents selected from G ² and/or Z ² ; or

III) a G ² group;

G ² represents, on each occasion when mentioned above, halo, cyano, -N ₃ ,

-NO ₂ , -ONO ₂ or -A ⁶ -R ^18a ; wherein A ⁶ represents a single bond or a spacer group selected from

-C(O)A ⁷ -, -S-, -S(O) ₂ A ⁸ -, -N(R ^19a )A ⁹ - or -OA ¹⁰ -, in which:

A ⁷ represents a single bond, -0-, -N(R ^19b )- or -C(O)-;

A ⁸ represents a single bond, -O- or -N(R ^19c )-;

A ⁹ and A ¹⁰ independently represent a single bond, -C(O)-, -C(0)N(R ^19d )-, -C(O)O-, -S(O) ₂ - or -S(O) ₂ N(R ¹⁹⁶ )-;

Z ² represents, on each occasion when mentioned above, =0, =S, =N0R ^18b , =NS(O) ₂ N(R ^19f )R ^18c , =NCN or =C(H)NO ₂ ;

R ^16a R ^16b R ^16c R ^17a R ^17b R ^17c R ^17d R ^17e R ^17f R ^18a R ^18b R ^18c R ^19a R ^19b R ^19c R ^19d , R ^19e and R ^19f are independently selected from: i) hydrogen; ii) an aryl group or a heteroaryl group, both of which are optionally substituted by one or more substituents selected from G ³ ;

iii) C _1-8 alkyl or a heterocycloalkyl group, both of which are optionally substituted by one or more substituents selected from G ³ and/or Z ³ ; or any pair of R ^16a to R ^16c and R ^17a to R ^17f , and/or R ^18a to R ^18c and R ^19a to R ^19f , may, for example when present on the same or on adjacent atoms, be linked together to form with those, or other relevant, atoms a further 3- to 8-membered ring, optionally containing 1 to 3 heteroatoms and/or 1 to 3 double bonds, which ring is optionally substituted by one or more substituents selected from G ³ and/or Z ³ ;

G ³ represents, on each occasion when mentioned above, halo, cyano, -N ₃ , -NO ₂ , -ONO ₂ or -A ¹¹ -R ^20a ; wherein A ¹¹ represents a single bond or a spacer group selected from -C(O)A ¹² -,

-S-, -S(O) ₂ A ¹³ -, -N(R ^21a )A ¹⁴ - or -OA ¹⁵ -, in which:

A ¹² represents a single bond, -O-, -N(R ²¹⁶ )- or -C(O)-;

A ¹³ represents a single bond, -O- or -N(R ^21c )-; A ¹⁴ and A ¹⁵ independently represent a single bond, -C(O)-, -C(O)N(R ²¹ ")-,

-C(O)O-, -S(O) ₂ - or -S(O) ₂ N(R ²¹⁶ )-;

Z ³ represents, on each occasion when mentioned above, =0, =S, =NOR ^20b , =NS(O) ₂ N(R ^21f )R ^20c , =NCN or =C(H)N0 ₂ ;

R ^20a , R ^20b , R ^2Oc , R ^21a , R ^21b , R ^21c , R ^21d , R ^21e and R ^21f are independently selected from: i) hydrogen; ii) C _1-6 alkyl or a heterocycloalkyl group, both of which groups are optionally substituted by one or more substituents selected from halo, Ci _-4 alkyl, -N(R ^22a )R ^23a , -OR ^22b and =0; and iii) an aryl or heteroaryl group, both of which are optionally substituted by one or more substituents selected from halo, Ci _-4 alkyl (optionally substituted by one or more substituents selected from =0, fluoro and chloro), -N(R ^22c )R ^23b and -OR ^22d ; or any pair of R ^20a to R ^20c and R ^21a to R ^21f may, for example when present on the same or on adjacent atoms, be linked together to form with those, or other relevant, atoms a further 3- to 8-membered ring, optionally containing 1 to 3 heteroatoms and/or 1 or 2 double bonds, which ring is optionally substituted by

one or more substituents selected from halo, Ci _-4 alkyl, -N(R ^22e )R ^23c , -OR and =0;

L ¹ represents -N(R ^W )A ¹⁹ -; L ² represents -N(R ^Z )A ²⁰ -;

A ¹⁹ represents a single bond, -C(O)N(R ^W )-, -S(O) ₂ - or -CH ₂ -; A ²⁰ represents a single bond, -C(O)N(R ^Z )-, -S(O) ₂ - or -CH ₂ -;

provided that when A ¹⁹ represents -S(O) ₂ -, Y ¹ represents Ar ¹ , and when A ²⁰ represents -S(O) ₂ -, then Y ² represents Ar ² ;

R ^x , R ^y , R ^w and R ^z independently represent, on each occasion when used herein, H, Ci- ₁₄ alkyl (optionally substituted by one or more substituents selected from halo, -CN ₁ -N(R ^24a )R ^25a , -OR ^24b , =0, aryl and heteroaryl (which latter two groups are optionally substituted by one or more substituents selected from halo, Ci _-4 alkyl (optionally substituted by one or more substituents selected from fluoro, chloro and =0), -N(R ^24c )R ^25b and -OR ^24d ));

R ^22a , R ^22b , R ^22c , R ^22d , R ^22e , R ^22f , R ^23a , R ^23b , R ^23c , R ^24a , R ^24b , R ^24c , R ^24d , R ^25a and R ^25b are independently selected from hydrogen and Ci _-4 alkyl, which latter group is optionally substituted by one or more substituents selected from fluoro, chloro or =0,

or a pharmaceutically-acceptable salt thereof,

and further provided that, when X ¹ and X ² are not present, and:

(a) R ^x and R ^y independently represent H or methyl and L ¹ and L ² both represent -N(H)-CH ₂ -, then Ar ¹ and Ar ² do not both represent unsubstituted phenyl;

(b) R ^x and R ^y independently represent H or methyl optionally substituted by unsubstituted phenyl, or one of R ^x and R ^y represents H and the other

represents methyl, and L ¹ and L ² both represent -N(H)-S(0)2-, then Ar ¹ and Ar ² do not both represent 4-methylphenyl; and

(c) when R ^x and R ^y both represent H, and L ¹ and L ² both represent -N(H)-S(O) ₂ , then Ar ¹ and Ar ² do not both represent 1-hydroxynaphthyl,

which compounds and salts are referred to hereinafter as "the compounds of the invention".

Pharmaceutically-acceptable salts include acid addition salts and base addition salts. Such salts may be formed by conventional means, for example by reaction of a free acid or a free base form of a compound of formula I with one or more equivalents of an appropriate acid or base, optionally in a solvent, or in a medium in which the salt is insoluble, followed by removal of said solvent, or said medium, using standard techniques (e.g. in vacuo, by freeze-drying or by filtration). Salts may also be prepared by exchanging a counter-ion of a compound of the invention in the form of a salt with another counter-ion, for example using a suitable ion exchange resin.

Compounds of the invention may contain double bonds and may thus exist as E (entgegen) and Z {zusammen) geometric isomers about each individual double bond. All such isomers and mixtures thereof are included within the scope of the invention.

Compounds of the invention may also exhibit tautomerism. All tautomeric forms and mixtures thereof are included within the scope of the invention.

Compounds of the invention may also contain one or more asymmetric carbon atoms and may therefore exhibit optical and/or diastereoisomerism. Diastereoisomers may be separated using conventional techniques, e.g. chromatography or fractional crystallisation. The various stereoisomers may be isolated by separation of a racemic or other mixture of the compounds using conventional, e.g. fractional crystallisation or HPLC, techniques. Alternatively the desired optical isomers may be made by reaction of the appropriate optically active starting materials under conditions which will not cause racemisation or

24

11 epimerisation (i.e. a 'chiral pool' method), by reaction of the appropriate starting material with a 'chiral auxiliary' which can subsequently be removed at a suitable stage, by derivatisation (i.e. a resolution, including a dynamic resolution), for example with a homochiral acid followed by separation of the diastereomeric derivatives by conventional means such as chromatography, or by reaction with an appropriate chiral reagent or chiral catalyst all under conditions known to the skilled person. All stereoisomers and mixtures thereof are included within the scope of the invention.

Unless otherwise specified, C _1-q alkyl groups (where q is the upper limit of the range) defined herein may be straight-chain or, when there is a sufficient number (i.e. a minimum of two or three, as appropriate) of carbon atoms, be branched- chain, and/or cyclic (so forming a C _3-q -cycloalkyl group). Such cycloalkyl groups may be monocyclic or bicyclic and may further be bridged. Further, when there is a sufficient number (i.e. a minimum of four) of carbon atoms, such groups may also be part cyclic. Such alkyl groups may also be saturated or, when there is a sufficient number (i.e. a minimum of two) of carbon atoms, be unsaturated (forming, for example, a C _2-q alkenyl or a C _2-q alkynyl group).

The term "halo", when used herein, includes fluoro, chloro, bromo and iodo.

Heterocycloalkyl groups that may be mentioned include non-aromatic monocyclic and bicyclic heterocycloalkyl groups (which groups may further be bridged) in which at least one (e.g. one to four) of the atoms in the ring system is other than carbon (i.e. a heteroatom), and in which the total number of atoms in the ring system is between three and twelve (e.g. between five and ten). Further, such heterocycloalkyl groups may be saturated or unsaturated containing one or more double and/or triple bonds, forming for example a C _2-q heterocycloalkenyl (where q is the upper limit of the range) or a C _7-q heterocycloalkynyl group. C ₂ ^, heterocycloalkyl groups that may be mentioned - include 7-azabicyclo- [2.2.1]heptanyl, 6-azabicyclo[3.1.1]heptanyl, 6-azabicyclo[3.2.1]-octanyl, 8- azabicyclo[3.2.1]octanyl, aziridinyl, azetidinyl, dihydropyranyl, dihydropyridyl, dihydropyrrolyl (including 2,5-dihydropyrrolyl), dioxolanyl (including 1 ,3- dioxolanyl), dioxanyl (including 1,3-dioxanyl and 1 ,4-dioxanyl), dithianyl (including 1 ,4-dithianyl), dithiolanyl (including 1 ,3-dithiolanyl), imidazolidinyl, imidazolinyl,

morpholinyl, 7-oxabicyclo[2.2.1]heptanyl, 6-oxabicyclo[3.2.1]-octanyl, oxetanyl, oxiranyl, piperazinyl, piperidinyl, pyranyl, pyrazolidinyl, pyrrolidinonyl, pyrrolidinyl, pyrrolinyl, quinuclidinyl, sulfolanyl, 3-sulfolenyl, tetrahydropyranyl, tetrahydrofuranyl, tetrahydropyridyl (such as 1 ,2,3,4-tetrahydropyridyl and 1 ,2,3,6-tetrahydropyridyl), thietanyl, thiiranyl, thiolanyl, thiomorpholinyl, trithianyl

(including 1 ,3,5-trithianyl), tropanyl and the like. Substituents on heterocycloalkyl groups may, where appropriate, be located on any atom in the ring system including a heteroatom. Further, in the case where the substituent is another cyclic compound, then the cyclic compound may be attached through a single atom on the heterocycloalkyl group, forming a so-called "spiro'-compound. The point of attachment of heterocycloalkyl groups may be via any atom in the ring system including (where appropriate) a heteroatom (such as a nitrogen atom), or an atom on any fused carbocyclic ring that may be present as part of the ring system. Heterocycloalkyl groups may also be in the N- or S- oxidised form.

For the avoidance of doubt, the term "bicyclic" (e.g. when employed in the context of heterocycloalkyl groups) refers to groups in which the second ring of a two-ring system is formed between two adjacent atoms of the first ring. The term "bridged" (e.g. when employed in the context of heterocycloalkyl groups) refers to monocyclic or bicyclic groups in which two non-adjacent atoms are linked by either an alkylene or heteroalkylene chain (as appropriate).

Aryl groups that may be mentioned include C ₆ - _H (such as C _6- - _I3 (e.g. C _6-10 )) aryl groups. Such groups may be monocyclic or bicyclic and have between 6 and 14 ring carbon atoms, in which at least one ring is aromatic. C _6-M aryl groups include phenyl, naphthyl and the like, such as 1 ,2,3,4-tetrahydronaphthyl, indanyl, indenyl and fluorenyl. The point of attachment of aryl groups may be via any atom of the ring system. However, when aryl groups are bicyclic or tricyclic, they are linked to the rest of the molecule via an aromatic ring.

Heteroaryl groups that may be mentioned include those which have between 5 and 14 (e.g. 10) members. Such groups may be monocyclic, bicyclic or tricyclic, provided that at least one of the rings is aromatic and wherein at least one (e.g. one to four) of the atoms in the ring system is other than carbon (i.e. a heteroatom). Heterocyclic groups that may be mentioned include oxazolopyridyl

(including oxazolo[4,5-b]pyridyl, oxazolo[5,4-b]pyridyl and, in particular, oxazolo[4,5-c]pyridyl and oxazolo[5,4-c]pyridyl), thiazolopyridyl (including thiazolo[4,5-£)]pyridyl, thiazolo[5,4-ό]pyridyl and, in particular, thiazolo[4,5- c]pyridyl and thiazolo[5,4-c]pyridyl), preferably, benzothiadiazolyl (including 2,1 ,3- benzothiadiazolyl), isothiochromanyl and, more preferably, acridinyl, benzimidazolyl, benzodioxanyl, benzodioxepinyl, benzodioxolyl (including 1 ,3- benzodioxolyl), beπzofuranyl, benzofurazanyl, benzothiazolyl, benzoxadiazolyl (including 2,1 ,3-benzoxadiazolyl), benzoxazinyl (including 3,4-dihydro-2H-1 ,4- benzoxazinyl), benzoxazolyl, benzomorphoiinyl, benzoselenadiazolyl (including 2,1 ,3-benzoselenadiazolyl), benzothienyl, carbazolyl, chromanyl, cinnolinyl, furanyl, imidazolyl, imidazopyridyl (including imidazo[4,5-b]pyridyl, imidazo[5,4- b]pyridyl and, preferably, imidazo[1 ,2-a]pyridyl), indazolyl, indolinyl, indolyl, isobenzofuranyl, isochromanyl, isoindolinyl, isoindolyl, isoquinolinyl, isothiaziolyl, isoxazolyl, naphthyridinyl (including 1 ,6-naphthyridinyl or, preferably, 1 ,5-naphthyridinyl and 1 ,8-naphthyridinyl), oxadiazolyl (including 1,2,3- oxadiazolyl, 1 ,2,4-oxadiazolyl and 1 ,3,4-oxadiazolyl), oxazolyl, phenazinyl, phenothiazinyl, phthalazinyl, pteridinyl, purinyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridyl, pyrimidinyl, pyrrolyl, quinazolinyl, quinolinyl, quinolizinyl, quinoxalinyl, tetrahydroisoquinolinyl (including 1 ,2,3,4-tetrahydroisoquinolinyl and 5,6,7,8- tetrahydroisoquinolinyl), tetrahydroquinolinyl (including 1 ,2,3,4- tetrahydroquinolinyl and 5,6,7,8-tetrahydroquinolinyl), tetrazolyl, thiadiazolyl (including 1 ,2,3-thiadiazolyl, 1 ,2,4-thiadiazolyl and 1 ,3,4-thiadiazolyl), thiazolyl, thiochromanyl, thienyl, triazolyl (including 1 ,2,3-triazolyl, 1 ,2,4-triazolyl and 1 ,3,4-triazolyl) and the like. Substituents on heteroaryl groups may, where appropriate, be located on any atom in the ring system including a heteroatom. The point of attachment of heteroaryl groups may be via any atom in the ring system including (where appropriate) a heteroatom (such as a nitrogen atom), or an atom on any fused carbocyclic ring that may be present as part of the ring system. Heteroaryl groups may also be in the N- or S- oxidised form.

Heteroatoms that may be mentioned include phosphorus, silicon, boron, tellurium, selenium and, preferably, oxygen, nitrogen and sulphur.

For the avoidance of doubt, in cases in which the identity of two or more substituents in a compound of the invention may be the same, the actual

identities of the respective substituents are not in any way interdependent. For example, in the situation in which X ¹ and X ² both represent R ^3a , i.e. a Ci _-6 alkyl group optionally substituted as hereinbefore defined, the alkyl groups in question may be the same or different. Similarly, when groups are substituted by more than one substituent as defined herein, the identities of those individual substituents are not to be regarded as being interdependent. For example, when

X ¹ represents two optional substituents -R ^3a and -C(O)R ^3b in which R ^3b represents

R ^3a , then the identities of the two R ^3a groups are not to be regarded as being interdependent. Likewise, when Ar ¹ represents e.g. an aryl group substituted by G ¹ in addition to, for example, C _1-8 alkyl, which latter group is substituted by G ¹ , the identities of the two G ¹ groups are not to be regarded as being interdependent.

For the avoidance of doubt, X ¹ and X ² represent between one and three optional (i.e. X ¹ and X ² may not be present) substituents, which may be attached to any one of the three free positions of the benzene ring to which X ¹ and/or X ² (as appropriate) is attached.

For the avoidance of doubt, when a term such as "R ⁴⁸ to R ⁴¹ " is employed herein, this will be understood by the skilled person to mean R ^4a , R ^4b , R ^4c , R ^4d , R ⁴⁶ , R ^4f , R ⁴⁹ , R ^4h and R ⁴ ' inclusively.

For the avoidance of doubt, where it is stated herein that "any pair of R ^16a to R ^16c and R ^17a to R ^17f ... may ... be linked together", we mean that any one of R ^16a , R ^16b or R ^16c may be linked with any one of R ^17a , R ^17b , R ^17c , R ^17d , R ^17e or R ^17f to form a ring as hereinbefore defined. For example, R ^16a and R ^17b (i.e. when a G ¹ group is present in which G ¹ represents -A ¹ -R ^16a , A ¹ represents -C(O)A ² and A ² represents -N(R ^17b )-), or R ^16c and R ^17f , may be linked together with the nitrogen atom to which they are necessarily attached to form a ring as hereinbefore defined.

Further compounds of the invention that may be mentioned include those in which: when X ¹ or X ² represent -N(R^)C(O)R ⁴⁰ , and R ^4c represents R ^3a , then R ^3a represents a linear or branched d- ₆ alkyl group optionally substituted by one or

more substituents selected from F, Cl ₁ -CN, -N ₃ , =0, -0R ^6a , -N(R ^6b )R ^7b , -S(O) _n R ^6c , -S(O) ₂ N(R ^6d )R ^7d or -OS(O) ₂ N(R ^6e )R ^7e ;

X ¹ and X ² independently represent one or more optional substituents selected from halo, -R ^3a , -CN, -C(O)R ^3b , -C(O)OR ^3c , -C(O)N(R ^4a )R ^5a , -N(R ^4b )R ^5b , -N(R ^3e )C(O)N(R ^4d )R ^5d , -N(R ^3f )C(O)OR ^4e , -N ₃ , -NO ₂ , -N(R ³⁹ )S(O) ₂ N(R ^4f )R ^5f , -0R ^3h , -OC(O)N(R ⁴⁹ )R ^5g , -OS(O) ₂ R ³ ', -S(O) _m R ^3j , -N(R ^3k )S(O) ₂ R ^3m , -OC(O)R ³ⁿ , -OC(O)OR ³ ", -S(O) ₂ N(R ^4h )R ^5h and -OS(O) ₂ N(R ^4| )R ⁵ '.

Compounds of the invention that may be mentioned include those in which: when, for example, L ¹ represents -N(R ^W )A ¹⁹ - or L ² represents -N(R ^Z )A ²⁰ -; A ¹⁹ and A ²⁰ independently represent a single bond; and/or R ^w and R ^z independently represent H, then:

Y ¹ or Y ² (as appropriate) do not represent a benzimidazolyl (such as one attached to the L ¹ or L ² group via the imidazolyl moiety, e.g. benzimidazol-2-yl) group; when Y ¹ or Y ² represents heteroaryl, then it is preferably a monocyclic heteroaryl group or a bicyclic heteroaryl group containing 1 to 4 heteroatoms consisting of 1 , 3 or 4 nitrogen heteroatoms, 1 or 2 oxygen heteroatoms and/or 1 sulfur atom, for instance, the bicyclic heteroaryl group may contain 1 nitrogen, oxygen or sulfur heteroatom (all of which are optionally substituted by one or more substituents selected from A); when Y ¹ or Y ² represents a polycyclic (e.g. bicyclic) heteroaryl group, then it is preferably not attached to the L ² or L ³ group via a ring containing a heteroatom; Y ¹ and/or Y ² (as appropriate) represent(s) aryl or a 5- or 6-membered monocyclic ring (all of which are optionally substituted by one or more substituents selected from A).

Preferred compounds of the invention include those in which R ^x , R ^y , R ^w and R ^z independently represent H, C _1-10 (e.g. C _1-8 ) alkyl (optionally substituted by one or more substituents selected from halo, -CN, -N(R ^24a )R ^25a , -OR ^24b or =0).

Compounds of the invention that may be mentioned include those in which A ¹⁹ represents -C(O)N(R")- and A ²⁰ represents -C(O)N(R ² )-. Preferred such compounds include those in which R ^w and R ^z are both H (at each occurrence).

Compounds of the invention that may also be mentioned include those in which A ¹⁹ and A ²⁰ both represent single bonds.

Other compounds of the invention that may be mentioned include those in which:

(a) A ¹⁹ does not represent -C(O)N(R")- and A ²⁰ does not represent -C(O)N(R ² )- (for example, A ¹⁹ does not represent -C(O)N(H)- and A ²⁰ does not represent -C(O)N(R ² )-); and

(b) A ¹⁹ and A ²⁰ do not both represent single bonds.

In this respect, compounds of the invention that may be mentioned include those in which:

(i) A ¹⁹ represents -C(O)N(R ^W )- and A ²⁰ represents -C(O)N(R ² )-, in which at least one of R ^w and R ^z represents C _1-14 alkyl (optionally substituted by one or more substituents selected from halo, -CN, -N(R ^24a )R ^25a , -OR ^24b , =O, aryl and heteroaryl (which latter two groups are optionally substituted by one or more substituents selected from halo, C _1-4 alkyl (optionally substituted by one or more substituents selected from fluoro, chloro and

=0), -N(R ^24c )R ^25b and -OR ^24d ));

(ii) A ¹⁹ represents -C(0)N(R ^w )- and A ²⁰ represents a single bond, -S(O) ₂ - or

-CH ₂ -;

(iii) A ²⁰ represents -C(O)N(R ² )- and A ¹⁹ represents a single bond, -S(O) ₂ - or

-CH ₂ -;

(iv) A ¹⁹ represents a single bond and A ²⁰ represents -C(O)N(R ² )-, -S(O) ₂ - or - CH ₂ -; and

(v) A ²⁰ represents a single bond and A ¹⁹ represents -C(O)N(R ^W )-, -S(O) ₂ - or - CH ₂ -.

Further compounds of the invention that may be mentioned include those in which:

M ¹ and M ² independently represent -CH ₃ , -CF ₃ or -N(R ^l4a )R ^15a ; R ^8a and R ^11a independently represent H ₁ -CH ₃ , -CH ₂ CH ₃ or -CF ₃ .

Preferred compounds of the invention include those in which: X ¹ and X ² independently represent one or more optional substituents selected from halo (e.g. chloro), R ^3a and -OR ^3h ;

X ¹ and X ² are the same (i.e. they are both absent or, when present, X ¹ and X ² represent the same substituent(s)); R ^4e represents R ^3a ; when any of the pairs R ⁴³ and R ^5a , R ^4b and R ^5b , R^ and R ^5d , R ^4f and R ^5f , R ^4g and R ^5g , R ^4h and R ^5h or R ⁴ ' and R ⁵ ' are linked together, they form a 5- or 6-membered ring optionally substituted by Cl ₁ =0 or, preferably, F or R ^3a ; R ^3c and R ^3j independently represent R ^3a ;

R ^3a represents C _1-6 (e.g. C _1-4 ) alkyl optionally substituted by one or more substituents selected from Cl, -N ₃ , =0, -N(R ^6b )R ^7b and, preferably, F and -OR ^6a ; m and n independently represent 2;

R ^6a , R ^6b , R ^6c , R ^6d and R ^6e independently represent H or C _1-3 alkyl optionally substituted by one or more fluoro atoms;

R ^7b , R ^7d and R ^7e independently represent H ₁ -S(O) ₂ CH ₃ , -S(O) ₂ CF ₃ or C _1-3 alkyl optionally substituted by one or more fluoro atoms, or the relevant pairs (i.e. R ^6b and R ^7b , R ^6d and R ^7d or R ^6e and R ^7e ) are linked together as defined herein; when R ^6b and R ^7b , R ^6d and R ^7d or R ^6e and R ^7e are linked together, they form a 5- or 6-membered ring, optionally substituted by F, Cl, =0 or -CH ₃ ; M ¹ and M ² independently represent -CH ₃ or -CF ₃ ;

R ^8a , R ^9a , R ^1Oa , R ^11a , R ^12a , R ^13a , R ^14a and R ^15a independently represent H or -CH ₃ ; A represents aryl (e.g. phenyl) optionally substituted by B; C _1-6 alkyl optionally substituted by G ¹ and/or Z ¹ ; or G ¹ ; G ¹ represents halo, cyano, N ₃ , -NO ₂ or -A ¹ -R ^16a ; A ¹ represents -C(O)A ² , -N(R ^17a )A ⁴ - or -OA ⁵ -; A ² represents a single bond or -0-;

A ⁴ represents -C(0)N(R ^17d )-, -C(O)O- or, more preferably, a single bond or -C(O)-; A ⁵ represents -C(O)- or, preferably, a single bond;

T/GB2008/000724

18

Z ¹ represents =NOR ^16b , =NCN or, preferably, =0;

B represents aryl (e.g. phenyl) optionally substituted by G ² ; C _1-6 alkyl optionally substituted by G ² and/or Z ² ; or, preferably G ² ,

G ² represents cyano or, more preferably, halo, -NO ₂ or -A ⁶ -R ^18a ; A ⁶ represents a single bond, -N(R ^19a )A ⁹ - or -OA ¹⁰ -;

A ⁹ represents -C(O)N(R ^19d )-, -C(O)O- or, more preferably, a single bond or -C(O)-;

A ¹⁰ represents a single bond;

Z ² represents =NOR ^18b , =NCN or, more preferably, =0; R ^16a R ^16b R ^16c R ^17a R ^17b R ^17c R ^17d R ^17e R ^17f R ^18a R ^18b R ^18c R ^19a R ^19b R ^19c R ^19d , R ^19e and R ^19f are independently selected from hydrogen, aryl (e.g. phenyl) or heteroaryl (which latter two groups are optionally substituted by G ³ ) or Ci _-6 (e.g. C _1-4 ) alkyl (optionally substituted by G ³ and/or Z ³ ), or the relevant pairs are linked together as hereinbefore defined; when any pair of R ^16a to R ^16c and R ^17a to R ^17f , or R ^18a to R ^18c and R ^19a to R ^19f are linked together, they form a 5- or 6-membered ring, optionally substituted by one or more (e.g. one or two) substituents selected from G ³ and/or Z ³ ; G ³ represents halo or -A ¹¹ -R ^20a ; A ¹¹ represents a single bond or -OA ¹⁵ -; A ¹⁵ represents a single bond; Z ³ represents =0; Pj ₂ Oa ₁ R ₂ Ob ₁ PJ ₂ Oc ₁ Pj ₂ Ia _{1 R} 2i _{b> R21CI} R ₂ Id _{1 R} 2i ^β _{and R} 2if _{are inde} p _e ndently selected from H or C _1-3 (e.g. C _1-2 ) alkyl (e.g. methyl) optionally substituted by one or more halo (e.g. fluoro) atoms, or the relevant pairs are linked together as defined herein; when any pair of R ^20a to R ^2Oc and R ^21a to R ^21f are linked together, they form a 5-,or

6-membered ring, optionally substituted by one or more (e.g. one or two) substituents selected from halo and Ci _-2 alkyl (e.g. methyl);

R ^x , R ^y , R ^w and R ^z independently represent H or C _1-6 (e.g. C _1-3 ) alkyl optionally substituted as defined herein, for example by one or more halo (e.g. fluoro) groups;

R ^x and R ^y are the same;

R ^w and R ^z are the same;

p22a p22b p22c p22d p22e p22f p23a p23b p23c p24a p24b p24c p24d p25a _an( -| p25b independently represent hydrogen or C _1-2 alkyl optionally substituted by =0 or, more preferably, one or more fluoro atoms.

Preferred aryl and heteroaryl groups that Ar ¹ and Ar ² may represent include optionally substituted (i.e. by A) phenyl, naphthyl, pyrrolyl, furanyl, thienyl (e.g. thien-2-yl or thien-3-yl), imidazolyl (e.g. 2-imidazolyl or 4-imidazolyl), oxazolyl, isoxazolyl, thiazolyl, pyrazolyl, pyridyl (e.g. 2-pyridyl, 3-pyridyl or 4-pyridyl), indazolyl, indolyl, indolinyl, isoindolinyl, quinolinyl, 1 ,2,3,4-tetrahydroquinolinyl, isoquinolinyl, 1 ,2,3,4-tetrahydroisoquinolinyl, quinolizinyl, benzofuranyl, isobenzofuranyl, chromanyl, benzothienyl, pyridazinyl, pyrimidinyl, pyrazinyl, indazolyl, benzimidazolyl, quinazolinyl, quinoxalinyl, 1 ,3-benzodioxolyl, tetrazolyl, benzothiazolyl, and/or benzodioxanyl, group. Preferred values include optionally substituted thienyl, thiazolyl or pyridyl or, more preferably, optionally substituted naphthyl (e.g. 1 -naphthyl or 2-naphthyl) or phenyl.

Preferred substituents on Ar ¹ and Ar ² groups include: halo (e.g. fluoro, chloro or bromo); cyano; -NO ₂ ;

C _1-6 alkyl, which alkyl group may be cyclic (e.g. cyclohexyl), part-cyclic, unsaturated or, preferably, linear or branched (e.g. C _1-4 alkyl (such as ethyl, n- propyl, isopropyl, π-butyl, f-butyl or, preferably, methyl), all of which are optionally substituted with one or more halo (e.g. fluoro) groups (so forming, for example, fluoromethyl, difluoromethyl or, preferably, trifluoromethyl); heterocycloalkyl, such as a 5- or 6-membered heterocycloalkyl group, preferably containing a nitrogen atom and, optionally, a further nitrogen or oxygen atom, so forming for example morpholinyl (e.g. 4-morpholinyl), piperazinyl (e.g. 4- piperazinyl) or piperidinyl (e.g. 1-piperidinyl and 4-piperidinyl) or pyrrolidinyl (e.g. 1 -pyrrolidinyl), which heterocycloalkyl group is optionally substituted by one or more (e.g. one or two) substituents selected from C _1-3 alkyl (e.g. methyl) and =0; -OR ²⁶ ; -C(O)OR ²⁶ : -C(O)R ²⁶ ; and -N(R ²⁶ )R ²⁷ ;

T/GB2008/000724

20 wherein R ²⁶ and R ²⁷ independently represent, on each occasion when mentioned above, aryl (e.g. phenyl) optionally substituted by one or more halo or C _1-3 (e.g. C _1-2 ) alkyl groups (which alkyl group is optionally substituted by one or more halo (e.g. fluoro) atoms) or, more preferably, H or C _1-6 alkyl, such as C _1-4 alkyl (e.g. ethyl, n-propyl, n-butyl, f-butyl or, preferably, methyl or isopropyl) optionally substituted by one or more halo (e.g. fluoro) groups (so forming e.g. a trifluoromethyl group).

Preferred compounds of the invention (particularly in those compounds in which A ¹⁹ and A ²⁰ both represent single bonds) include those in which:

Y ¹ and Y ² independently (i.e. either one or, more preferably, both) do not represent H; when Ar ¹ and Ar ² are substituted, they are preferably substituted by one to three

(e.g. one or two) substituents as defined herein; A represents G ¹ or C _1-4 alkyl (e.g. f-butyl or methyl) optionally substituted by one or more G ¹ groups (e.g. by halo, such as fluoro);

G ¹ represents halo (e.g. F or Cl) or -A ¹ -R ^16a ;

A ¹ represents a single bond or, more preferably, -C(O)A ² - or -OA ⁵ -;

A ² represents -O-; A ⁵ represents a single bond;

R ^16a represents aryl (e.g. phenyl) or heteroaryl, which are both optionally substituted by one or more G ³ groups or, more preferably, H or C _1-6 alkyl (e.g. cyclohexyl or, more preferably, C _1-2 alkyl) optionally substituted by one or more G ³ (e.g. fluoro) substituents; G ³ represents fluoro or -A ¹¹ -R ^20a ;

X ¹ and X ² independently represent halo (e.g. chloro) or is/are not present; when X ¹ and X ² is/are present, they independently represent two or, preferably, one substituent as defined herein; when X ¹ and X ² are present, they represent one substituent (as defined herein) preferably attached to the position α to the -N(R ^Z )-Y ¹ or -N(R ^W )-Y ² substituent in the compound of formula I;

Ar ¹ and Ar ² independently represent phenyl or naphthyl optionally substituted as defined herein;

when Ar ¹ and Ar ² represent a phenyl group, it may be unsubstituted or substituted with one substituent or with two substituents (so forming, for example a 2,3-, a 3,5-, a 3,4- or a 2,4-substitution pattern) as defined herein; when Ar ¹ or Ar ² represents naphthyl, it is preferably unsubstituted; Ar ¹ and Ar ² are the same;

R ^x and R ^y independently represent H;

R ^w and R ^z independently represent H or C _1-3 (e.g. C _1-2 ) alky! (e.g. n-propyl or, more preferably, methyl), which group may be optionally substituted by a phenyl group, optionally substituted by C _1-3 alkyl, such as methyl.

Particularly preferred substituents on Ar ¹ and Ar ² groups (particularly in those compounds in which A ¹⁹ and A ²⁰ represent single bonds) include, for example, one or more substituents selected from cyclohexyl or, more preferably, halo (e.g. chloro, fluoro or bromo), -C(O)OH, -CH ₃ , -CF ₃ , f-butyl, -OCH ₃ , -OCF ₃ or -O-isopropyl substituents.

In addition to the above-mentioned preferences, preferred compounds of the invention (particularly in those compounds in which A ¹⁹ and A ²⁰ both represent

-C(O)N(H)-, or one of A ¹⁹ or A ²⁰ represents -C(O)N(H)- and the other represents a single bond and Y ¹ and/or Y ² (as appropriate) represents H) may also include those in which: when Ar ¹ and Ar ² are substituted, they are preferably substituted by one to three

(e.g. two or, more preferably, one) substituents as defined herein;

A represents G ¹ or C _1-3 alkyl (e.g. methyl) optionally substituted by one or more G ¹ groups (e.g. halo, such as fluoro);

G ¹ represents halo (e.g. fluoro or chloro), cyano, -NO ₂ or -A ¹ -R ^16a ;

A ¹ represents -C(O)A ² - or -OA ⁵ -;

A ² and A ⁵ independently represent a single bond;

R ^16a represents C _1-4 (e.g. C _1-2 ) alkyl (e.g. n-butyl or methyl) or an aryl (e.g. phenyl) or heteroaryl group, which latter two are optionally substituted by one or more G ³ groups;

Ar ¹ and Ar ² independently represent phenyl optionally substituted as defined herein.

Particularly preferred substituents on Ar ¹ and Ar ² groups (particularly in those compounds those in which A ¹⁹ and A ²⁰ both represent -C(O)N(H)-, or one of A ¹⁹ or A ²⁰ represents -C(O)N(H)- and the other represents a single bond and Y ¹ and/or Y ² (as appropriate) represents H) include, for example, one or more substituents selected from halo (e.g. chloro, fluoro or bromo), cyano, -C(O)CH ₃ , -CH ₃ , -CF ₃ , -NO ₂ , -OCH ₃ , -O-n-butyl and -O-phenyl (i.e. phenoxy).

Preferred compounds of the invention include those in which A ¹⁹ and/or A ²⁰ represent -CH ₂ - or, more preferably, a single bond, or -C(O)N(R ^W )- or -C(O)N(R ² )- (as appropriate).

Compounds of the invention that may be mentioned include those in which A ¹⁹ and A ²⁰ are both the same. Other compounds of the invention that may be mentioned include those in which one of A ¹⁹ or A ²⁰ represents -S(O) ₂ - and the other represents -C(O)N(R ^W )- or -C(O)N(R ² )- (as appropriate).

Compounds of the invention that may be mentioned (particularly in those compounds in which A ¹⁹ and A ²⁰ both represent -S(O) ₂ -) also include those in which: when Ar ¹ and Ar ² are substituted, they are preferably substituted by one to two substituents as defined herein;

A represents G ¹ or C _1-4 alkyl (preferably π-butyl or methyl), optionally substituted by one or more (e.g. three) G ¹ groups (such as halo, e.g. fluoro));

G ¹ represents halo (e.g. fluoro or chloro), cyano, -NO ₂ or -A ¹ -R ^16a ; A ¹ represents a single bond, -N(R ^17a )A ⁴ , -C(O)A ² - or -0-A ⁵ -;

A ² represents -0-;

A ⁴ represents -C(O)- or a single bond;

A ⁵ represents a single bond;

R ^16a represents H or C _1-4 alkyl (e.g. C _1-2 alkyl), optionally substituted by one or more (e.g. three) G ³ (e.g. fluoro) substituents);

R ^17a represents H;

Ar ¹ and Ar ² independently represent phenyl or naphthyl optionally substituted as defined herein (the latter being preferably unsubstituted).

Particularly preferred substituents on Ar ¹ and Ar ² groups (particularly in .those compounds in which A ¹⁹ and A ²⁰ represent -S(O) ₂ -) include, for example, one or more substituents selected from halo (e.g. chloro or fluoro), cyano, -NO ₂ , -C(O)OH ₁ -CF ₃ , -OCH ₃ , -OCF ₃ , -NH ₂ , -N(H)-C(O)CH ₃ , -n-butyl and -O-π-butyl.

Compounds of the invention that may be mentioned (particularly in those compounds in which A ¹⁹ and A ²⁰ both represent -CH ₂ -) may also include those in which:

when Ar ¹ and Ar ² are substituted, they are preferably substituted by one to two substituents as defined herein;

A represents G ¹ or C _1-4 alkyl (preferably methyl, which is optionally substituted by one or more (e.g. three) G ¹ groups (such halo, e.g. fluoro));

G ¹ represents halo (e.g. fluoro or chloro) or -A ¹ -R ^16a , A ¹ represents -0-A ⁵ -;

A ⁵ represents a single bond;

R ^16a represents C _1-4 alkyl (preferably C _1-2 alkyl), optionally substituted by one or more (e.g. three) G ³ groups (e.g. fluoro or -A ¹¹ -R ^2Oa );

A ¹¹ represents a single bond; R ^2Oa represents and aryl (e.g. phenyl);

Ar ¹ and Ar ² independently represent phenyl optionally substituted as defined herein.

Particularly preferred substituents on Ar ¹ and Ar ² groups (particularly in those compounds in which A ¹⁹ and A ²⁰ represent -S(O) ₂ -) include, for example, one or more substituents selected from halo (e.g. chloro or fluoro), -CF ₃ , -OCH ₃ , -CH ₃ and -O-CH ₂ -phenyl.

Compounds of the invention that may be mentioned (particularly in those compounds in which one of A ¹⁹ or A ²⁰ represents -S(O) ₂ - and the other represents

-C(O)N(H)-) may also include those in which: when Ar ¹ and Ar ² are substituted, they are preferably substituted by one to two substituents as defined herein;

A represents G ¹ ; G ¹ represents halo (e.g. fluoro or chloro) or -NO ₂ ;

24

Ar ¹ and Ar ² independently represent phenyl optionally substituted as defined herein.

Particularly preferred substituenfs on Ar ¹ and Ar ² groups (particularly in those compounds in which one of A ¹⁹ or A ²⁰ represents -S(O) ₂ - and the other represents -C(O)N(H)-) include, for example, one or more substituents selected from halo (e.g. chloro) and -NO ₂ .

Particularly preferred compounds of the invention include those of the examples described hereinafter.

Compounds of the invention may be made in accordance with techniques that are well known to those skilled in the art, for example as described hereinafter.

According to a further aspect of the invention there is provided a process for the preparation of a compound of formula I which process comprises:

(i) for compounds of formula I in which A ¹⁹ and A ²⁰ represent a single bond, and in particular for the preparation of compounds of formula I in which R ^x and R ^y do not represent hydrogen, reaction of a compound of formula II,

or a protected (e.g. at one of the amino groups) derivative thereof, wherein R* and R ^y are as hereinbefore defined but preferably do not represent hydrogen, and X ¹ , X ² , R ^w and R ^z are as hereinbefore defined, with a compound of formula III,

tκf-l ^a

wherein Ar ²¹ represents Ar ¹ or Ar ² (as appropriate/required) and L ^a represents a suitable leaving group such as chloro, bromo, iodo, a sulfonate group (e.g.

-OS(O) ₂ CF ₃ , -OS(O) ₂ CH ₃ , -OS(O) ₂ PhMe or a nonaflate) or

-B(OH) ₂ and Ar ¹ and Ar ² are as hereinbefore defined, for example optionally in the presence of an appropriate metal catalyst (or a salt or complex thereof) such as Cu, Cu(OAc) ₂ , CuI (or Cul/diamine complex), copper tris(triphenyl- phosphine)bromide, Pd(OAc) ₂ , Pd ₂ (dba) ₃ or NiCI ₂ and an optional additive such as Ph ₃ P, 2,2'-bis(diphenylphosphino)-1 ,1'-binaphthyl, xantphos, NaI or an appropriate crown ether such as 18-crown-6-benzene, in the presence of an appropriate base such as NaH, Et ₃ N, pyridine, λ/./V-dimethylethylenediamine,

Na ₂ CO ₃ , K ₂ CO ₃ , K ₃ PO ₄ , Cs ₂ CO ₃ , NBuONa or NBuOK (or a mixture thereof, optionally in the presence of 4A molecular sieves), in a suitable solvent (e.g. dichioromethane, dioxane, toluene, ethanol, isopropanol, dimethylformamide, ethylene glycol, ethylene glycol dimethyl ether, water, dimethylsulfoxide, acetonitrile, dimethylacetamide, λ/-methylpyrrolidinone, tetrahydrofuran or a mixture thereof) or in the absence of an additional solvent when the reagent may itself act as a solvent (e.g. when Ar ³ represents phenyl and L ^a represents bromo, i.e. bromobenzene). This reaction may be carried out at room temperature or above (e.g. at a high temperature, such as the reflux temperature of the solvent system that is employed) or using microwave irradiation. The skilled person will appreciate that this preparation may result in compounds of formula I in which one of Y ¹ and Y ² represents H, or neither of Y ¹ or Y ² represent H. Hence, the desired products may be separated in accordance with standard techniques. Compounds in which one of Y ¹ or Y ² represent H may be prepared in higher yields by either employing less than two equivalents of a compound of formula III in the reaction mixture, or by employing a mono-protected (at a single amino group) compound of formula II. Compounds of formula I in which neither Y ¹ or Y ² represent H may be prepared in higher yield by employing an excess (i.e. more than two equivalents) of (a) compound(s) of formula III in the reaction mixture;

(ii) for compounds of formula I in which R ^w and/or R ^z do not represent hydrogen, reaction of a corresponding compound of formula I in which R ^w and/or R ^z (as appropriate) do represent hydrogen with a compound of formula IV,

R^-L" IV

wherein FT ² represents either R ^w or R ^z (as appropriate) as hereinbefore defined provided that it/they does/do not represent hydrogen, and L ^b represents a suitable leaving group such as one hereinbefore defined in respect of L ^a or -Sn(alkyl) ₃ (e.g. -SnMe ₃ or -SnBu ₃ ), or a similar group known to the skilled person, under reaction conditions known to those skilled in the art, for example such as those described in respect of process step (i) above or, for example in the case where L ^b represents a leaving group such as iodo, bromo, chloro or a sulfonate group, the reaction may be performed at around room temperature or above (e.g. up to 40-180 ⁰ C), optionally in the presence of a suitable base (e.g. sodium hydride, sodium bicarbonate, potassium carbonate, pyrrolidinopyridine, pyridine, triethylamine, tributylamine, trimethylamine, dimethylaminopyridine, diisopropylamine, diisopropylethylamine, 1 ,8-diazabicyclo[5.4.0]undec-7-ene, sodium hydroxide, λ/-ethyldiisopropylamine, λ/-(methylpolystyrene)-4- (methylamino)pyridine, potassium bis(trimethylsilyl)amide, sodium bis(thmethylsilyl)amide, potassium terf-butoxide, lithium diisopropylamide, lithium 2,2,6,6-tetramethylpiperidine or mixtures thereof) and an appropriate solvent (e.g. tetrahydrofuran, pyridine, toluene, dichloromethane, chloroform, acetonitrile, dimethylformamide, trifluoromethylbenzene, dioxane or triethylamine). In the case when L ^b represents -B(OH) ₂ or -Sn(alkyl) ₃ , the reaction may be performed in the presence of a suitable catalyst system, e.g. a metal (or a salt or complex thereof) such as CuI, Pd/C, PdCI ₂ , Pd(OAc) ₂ , Pd(Ph ₃ P) ₂ CI ₂ , Pd(Ph ₃ P) ₄ , Pd ₂ (dba) ₃ or NiCI ₂ and a ligand such as J-Bu ₃ P, (C ₆ Hn) ₃ P, Ph ₃ P, AsPh ₃ , P(O-ToI) ₃ , 1 ,2- bis(diphenylphosphino)ethane, 2,2'-bis(di-terf-butylphosphino)-1 ,1'-bi-phenyl, 2,2'- bis(diphenylphosphino)-1 ,1'-bi-naphthyl, 1 ,1'-bis(diphenylphosphinoferrocene), 1 ,3-bis(diphenylphosphino)-propane, xantphos, or a mixture thereof, together with a suitable base such as, Na ₂ CO ₃ , K ₃ PO ₄ , Cs ₂ CO ₃ , NaOH, KOH, K ₂ CO ₃ , CsF, Et ₃ N, (/-Pr) ₂ NEt, NBuONa or f-BuOK (or mixtures thereof) in a suitable solvent such as dioxane, toluene, ethanol, dimethylformamide, ethylene glycol dimethyl ether, water, dimethylsulfoxide, acetonitrile, dimethylacetamide, N- methylpyrrolidinone, tetrahydrofuran or mixtures thereof. Further, the skilled person will appreciate that FC ² may be contain a double bond, for example α to the L ^b substituent (which double bond may migrate after reaction). In this instance, it may be desired to subsequently reduce the double bond to provide a saturated R^ group, for example as described hereinafter;

(iii) for compounds of formula I that contain only saturated alkyl groups (for example, when R ^w and/or R ^z represent optionally substituted saturated C _1-14 alkyl), reduction of a corresponding compound of formula I that contains an unsaturation, such as a double or triple bond (e.g. for compounds of formula I in which R ^w and/or R ^z represent C _2-14 alkenyl), in the presence of suitable reducing conditions, for example by catalytic (e.g. employing Pd) hydrogenation;

(iv) for compounds of formula I that contain amine groups (for example, where G ¹ represents -NH ₂ , or, for compounds of formula I in which either -L ¹ -Y ¹ or -L ² - Y ² represents -NH ₂ ) reduction of a corresponding compound of formula I that contains a group that may be reduced to an amine group, such a nitro or azide group (e.g. G ¹ represents -NO ₂ or -N ₃ ), in the presence of suitable reducing conditions, for example by catalytic (e.g. employing Pd) hydrogenation or employing an appropriate reducing agent (such as trialkylsilane, e.g. triethylsilane). The skilled person will also appreciate that the amine, once formed, may further be substituted (e.g. alkylated) using any appropriate process, for example those described herein;

(v) for compounds of formula I in which A ¹⁹ and A ²⁰ independently represent a single bond or -CH ₂ -, and R ^w and/or R ² represents optionally substituted C _2-14 alkyl, reductive amination of a compound of formula Il as defined above, with a compound of formula V,

R"*=O V

wherein R^ ¹ represents C _1- - _I3 alkyl optionally substituted with the substituents hereinbefore defined in respect of R ^w and/or R ^z (and the compound of formula V is thus either an aldehyde or ketone). Reductive amination (which comprises condensation followed by reduction) reaction conditions are well known to those skilled in the art, for example, such reactions may be performed in the presence of a suitable chemoselective reducing agent, such as sodium cyanoborohydride, sodium triacetoxyborohydride or borane (or various complexes thereof). Alternatively, the reduction step may be performed as a completely separate step after the condensation step (which condensation step may itself be promoted when performed in the presence of a suitable reagent such as a titanium based

reagent, e.g. Ti(OZ-Pr) ₄ ), in the presence of a stronger reducing agent such as sodium borohydride or borane (and various complexes thereof);

(vi) reaction of a compound of formula Vl,

wherein Z ^x and Z ^y independently represent a suitable leaving group such as chloro, bromo, iodo, a sulfonate group (e.g. -OS(O) ₂ CF ₃ , -OS(O) ₂ CH ₃ , -OS(O) ₂ PhMe or a nonaflate), -B(OH) ₂ , -B(OR ⁿ ) _2l -Sn(R ^π ) ₃ or diazonium salts, in which each R ^π independently represents a Ci _-6 alkyl group, and R", R ^y , X ¹ and X ² are as hereinbefore defined, with a compound of formula VII,

y ^a -A ²¹ -NH ₂ VlI

wherein Y ⁸ is as hereinbefore defined, A represents A or A (as required/appropriate) (where A ¹⁹ or A ²⁰ preferably independently represent -N(H)- C(O)-N(H)- or a single bond) under suitable reaction conditions known to those skilled in the art, such as those described hereinbefore in respect of process step

(i);

(vii) for compounds of formula I in which A ¹⁹ and/or A ²⁰ represents -CH ₂ -, reductive amination of a compound of formula Il as defined above, in the presence of a compound of formula VIII,

Ar ³ CH=O VIII

wherein Ar ³ is as hereinbefore defined. Reductive amination (which comprises condensation followed by reduction) reaction conditions are well known to those skilled in the art, for example, those described hereinbefore in respect of process step (v);

(viii) for compounds of formula I in which A ¹⁹ and/or A ²⁰ represents -CH ₂ -, reaction of a compound of formula Il as defined above, with a compound of formula IX,

Ar ³ C(O)CI IX

wherein Ar* is as hereinbefore defined, under conditions known to one skilled in the art, for example, those described hereinbefore in respect of process step (ii), followed by reduction of the resulting compound (either in a separate reaction or in one pot), under conditions known to one skilled in the art, for example using a suitable reducing agent, such as borane (and various complexes thereof);

(ix) for compounds of formula I in which R ^x and R ^y represent hydrogen, hydrolysis of a corresponding compound of formula in which R ^x and R ^y do not represent hydrogen, or other carboxylic acid or ester protected derivatives (e.g. amide derivatives) thereof, under standard conditions, for example in the presence of an aqueous solution of base (e.g. aqueous 2M NaOH) optionally in the presence of an (additional) organic solvent (such as dioxane, diethyl ether or MeOH), which reaction mixture may be stirred at room or, preferably, elevated temperature (e.g. about 12O ⁰ C) for a period of time until hydrolysis is complete (e.g. 5 hours);

(x) for compounds of formula I in which R ^x and R ^y do not represent hydrogen (and are preferably the same), esterification of corresponding compounds of formula I in which R ^x and R ^y represent hydrogen (or trans-esterification of compounds of formula I in which R ^x and R ^y do not represent hydrogen or the same value of the corresponding R ^x and R ^y groups in the compound of formula I to be prepared), in the presence of a compound of formula X,

R ^b -OH X

wherein R ^b represents R ^x or R ^y (as appropriate/required) provided that it does not represent hydrogen, under standard conditions, for example in the presence of acid (e.g. concentrated H ₂ SO ₄ ) at elevated temperature, such as at the reflux temperature of the alcohol of formula X;

(xi) for compounds of formula I in which A ¹⁹ and A ²⁰ represent -S(O) ₂ - or -CH ₂ -, reaction of a compound of formula Il with a compound of formula Xl ₁

Y ³ ^-L ⁰ Xl

wherein Y ⁸ represents Ar ¹ or Ar ² (as appropriate/required) as hereinbefore defined and L ^c represents a suitable leaving group, for example, fluoro (especially when A ^x represents -S(O) ₂ -) or a suitable leaving group such as one defined hereinbefore in respect of L ^a , and A ^x represents either -CH ₂ - or -S(O) ₂ -, under suitable conditions as known to one skilled in the art, for example the reaction may be performed at around room temperature or above (e.g. up to 40-180 ⁰ C), optionally in the presence of a suitable base (e.g. sodium hydride, sodium bicarbonate, potassium carbonate, pyrrolidinopyridine, pyridine, triethylamine, tributylamine, trimethylamine, dimethylaminopyridine, diisopropylamine, diisopropylethylamine, 1 ,8-diazabicyclo[5.4.0]undec-7-ene, sodium hydroxide, N- ethyldiisopropylamine, /V-(methylpolystyrene)-4-(methylamino)pyridine, potassium bis(trimethylsilyl)amide, sodium bis(trimethylsilyl)amide, potassium tert- butoxide, lithium diisopropylamide, lithium 2,2,6,6-tetramethylpiperidine or mixtures thereof) and an appropriate solvent (e.g. tetrahydrofuran, pyridine, toluene, dichloromethane, chloroform, acetonitrile, dimethylformamide, trifluoromethylbenzene, dioxane or triethylamine). Alternatively, reaction conditions such as those described hereinbefore in respect of process step (ii) may be employed. The skilled person will appreciate that for the preparation of compounds of formula I in where either A ¹⁹ represents a single bond and Y ¹ represents H, or A ²⁰ represents a single bond and Y ² represents H, then a mono- protected (at a single amino group) compound of formula Il may be employed or the reaction may be performed with less than 2 equivalents of the compound of formula Xl. The skilled person will also appreciate that for preparation of compounds of formula I in which A ¹⁹ and A ²⁰ , and/or, Ar ¹ and Ar ² are different, two different compounds of formula Xl will need to be employed in successive reaction steps;

(xii) for compounds of formula I in which A ¹⁹ and A ²⁰ both represent -C(O)N(H)-, reaction of a compound of formula II, or a protected (e.g. at one of the amino groups) derivative thereof, with either:

24

31

(A) a compound of formula XII ₁

Y^N=C=O XII

; or

(B) with CO (or a reagent that is a suitable source of CO (e.g. Mo(CO) ₆ or Co ₂ (CO) ₈ )) in the presence of a compound of formula XIII,

Y^NH ₂ XIII

wherein, in both cases, Y ³¹ represents Ar ¹ or Ar ² (as appropriate/required) as hereinbefore defined. For example, in the case of (A) above, in the presence of a suitable solvent (e.g. THF, dioxane or diethyl ether) under reaction conditions known to those skilled in the art (e.g. at room temperature). In the case of (B), suitable conditions will be known to the skilled person, for example the reactions may be carried out in the presence of an appropriate catalyst system (e.g. a palladium catalyst), preferably under pressure and/or under microwave irradiation conditions. The skilled person will appreciate that the compound so formed may be isolated by precipitation or crystallisation (from e.g. n-hexane) and purified by recrystallisation techniques (e.g. from a suitable solvent such as THF, hexane (e.g. π-hexane), methanol, dioxane, water, or mixtures thereof). The skilled person will appreciate that for the preparation of compounds of formula I in which one of Y ¹ and Y ² represents H, then a mono-protected (at a single amino group) compound of formula Il may be employed or the reaction may be performed with less than 2 equivalents of the compound of formula XII or XIII (as appropriate). The skilled person will also appreciate that for preparation of compounds of formula I in which L ¹ -Y ¹ represents -N(R ^W )-C(O)N(R ^W )-Ar ¹ and L ² -Y ² represents -N(R ² J-C(O)N(R^-Ar ² , and L ¹ -Y ¹ and L ² -Y ² are different, two different compounds of formula XII or XIII (as appropriate) will need to be employed in successive reaction steps;

(xiii) for compounds of formula I in which A ¹⁹ and A ²⁰ both represent -C(O)N(H)-, reaction of a compound of formula XIV,

24

32

wherein R ^x , R ^y , X ¹ and X ² are as hereinbefore defined, with a compound of formula XIII as defined above, under reaction conditions known to those skilled in the art, such as those described hereinbefore in respect of process step (xii); or

(xiv) particularly for compounds of formula I in which R ^x and R ^y , X ¹ and X ² and Y ¹ and Y ² are the same, reaction of a compound of formula XV (or two different compounds of formula XV for preparation of compounds of formula I in which R ^x and R ^y , X ¹ and X ² and/or Y ¹ and Y ² are different),

wherein R ^a represents R ^x or R ^y (as required/appropriate and in which these substituents are preferably other than hydrogen and are preferably the same), L ³ represents L ¹ or L ² (as required/appropriate and in which these substituents are preferably the same), X ^a represents X ¹ or X ² (as required/appropriate and in which these substituents are preferably the same), Y ^a is as hereinbefore defined, with formaldehyde (e.g. in the form of paraformaldehyde or an aqueous solution of formaldehyde such as a 3% aqueous solution), for example under acidic conditions (e.g. in the presence of aqueous HCI) at or above room temperature (e.g. at between 50 ⁰ C and 70°C). Preferably, the formaldehyde is added (e.g. slowly) to an acidic solution of the compound of formula XV at about 50 ⁰ C, with the reaction temperature rising to about 7O ⁰ C after addition is complete. When acidic conditions are employed, precipitation of the compound of formula I may be effected by the neutralisation (for example by the addition of a base such as ammonia).

24

33

Compounds of formula Il (or protected, e.g. mono-protected derivatives thereof) may be prepared by reduction of a compound of formula XVI,

wherein Z ^z1 and Z ²² independently represent -N ₃ , -NO ₂ or one of Z ^z1 or Z ²² may represent a protected -NH ₂ group (for instance, in the case where appropriate mono-protected derivatives of compounds of formula Il are required) under standard reaction conditions known to those skilled in the art, in the presence of a suitable reducing agent, for example reduction by catalytic hydrogenation (e.g. in the presence of a palladium catalyst in a source of hydrogen) or employing an appropriate reducing agent (such as trialkylsilane, e.g. triethylsilane).

Compounds of formula Il (or protected derivatives thereof) may also be prepared by reaction of a compound of formula Vl as defined above, with ammonia, or preferably with a protected derivative thereof (e.g. benzylamine or Ph ₂ C=NH) ₁ under conditions such as those described hereinbefore in respect of preparation of compounds of formula I (process step (vi) above).

Compounds of formula Il or compounds of formula Vl may be prepared by:

(I) reaction of a compound of formula XVII,

wherein Z ^q1 and Z ^q2 respectively represent Z ^x and Z ^y (in the case of preparation of compounds of formula Vl) or -NH ₂ (or preferably a protected derivative thereof; in

B2008/000724

34 the case of preparation of compounds of formula II), one of W ¹ and W ² represents hydrogen and the other represents hydrogen or -C(O)OR ^X or -C(O)OR ^y (as appropriate), and X ¹ , X ² , R ^x , R ^y , Z ^x and Z ^y are as hereinbefore defined, with a suitable reagent such as phosgene or triphosgene in the presence of an appropriate base (e.g. triethylamine), followed by reaction in the presence of a compound of formula XVIII,

HO-R ^xy XVIII

wherein R ^xy represents R ^x or R ^y (as appropriate), hence undergoing a hydrolysis or alcoholysis reaction step;

(II) for compounds of formula Il or Vl in which R ^x and/or R ^y represent hydrogen, formylation of a compound of formula XVII as hereinbefore defined, for example in the presence of suitable reagents such as P(O)CI ₃ and DMF, followed by oxidation under standard conditions;

(III) reaction of a compound of formula XIX,

wherein one of W ³ and W ⁴ represents a suitable leaving group such as one defined by Z ^x and Z ^y above and the other also represents such a leaving group or -C(O)OR ^X or -C(0)0R ^y (as appropriate), and X ¹ , X ² , R ^x , R ^y , Z ^q1 and Z ^q2 are as hereinbefore defined, with CO (or a reagent that is a suitable source of CO (e.g. Mo(CO) ₆ or Co ₂ (CO) ₈ )) followed by reaction in the presence of a compound of formula XVIII as hereinbefore defined, under reaction conditions known to those skilled in the art, for example such as those hereinbefore described in respect of preparation of compounds of formula I (process step (xϋ)(B) above), e.g. the carbonylation step being performed in the presence of an appropriate precious metal (e.g. palladium) catalyst;

B2008/000724

35

(IV) reaction of a compound of formula XX,

wherein one of W ⁵ and W ⁶ represents a suitable group such as an appropriate alkali metal group (e.g. sodium, potassium or, especially, lithium), a -Mg-halide or a zinc-based group, the other one of W ⁵ or W ⁶ may also represent such as group or may represent -C(O)OR ^X or -C(O)OR ^y (as appropriate), and X ¹ , X ² , R ^x and R ^y are as hereinbefore defined, with e.g. CO ₂ (in the case where R ^x and/or R ^y in the compound of formula Il or Vl to be prepared represents hydrogen) or a compound of formula XXI,

LλC(O)OR ^xy XXI

wherein L ^z represents a suitable leaving group, such as chloro or bromo or a C ₁ - _I4 (such as C,_ ₅ (e.g. C _1-3 ) alkoxy group), and R ^xy is as hereinbefore defined, provided that it does not represent hydrogen, under reaction conditions known to those skilled in the art. The skilled person will appreciate that this reaction step may be performed directly after (i.e. in the same reaction pot) the preparation of compounds of formula XX.

Compounds of formula Vl in which Z ^x and Z ^y both represent a sulfonate group may be prepared by reaction of a compound of formula XXII,

wherein R ^x and R ^y are as hereinbefore defined (and preferably do not represent hydrogen) and X ¹ and X ² are as hereinbefore defined, with an appropriate

24

36 reagent for the conversion of the hydroxyl group to the sulfonate group (e.g. tosyl chloride, mesyl chloride, triflic anhydride and the like) under conditions known to those skilled in the art, for example in the presence of a suitable base and solvent (such as those described above in respect of process step (i), e.g. an aqueous solution of K ₃ PO ₄ in toluene) preferably at or below room temperature (e.g. at about 1O ⁰ C).

Compounds of formula XIV may be prepared by reaction of a corresponding compound of formula Il in which R ^z and R ^w represent hydrogen, with phosgene or triphosgene, for example in the presence of a suitable base (e.g. one hereinbefore defined in respect of preparation of compounds of formula I (process step (i), e.g. triethylamine). When the compound of formula XIV is synthesised accordingly, it need not be isolated and/or purified when further employed in the synthesis of a compound of formula I (see process step (xiii) above).

Compounds of formula XV in which L ³ is as hereinbefore defined (as required/appropriate) may be prepared by reduction of a compound of formula XXIII ₁

XXIII

o forming a corresponding compound of formula XXIIIA,

XXIIIA

wherein R ^a and X ^a are as hereinbefore defined, followed by reaction in the presence of a compound of formula III, Xl or XII (as appropriate) as hereinbefore defined, under reaction conditions such as those described herein.

Compounds of formula XXIII may be prepared by hydrolysis of a compound of formula XXIV,

wherein X ^a is as hereinbefore defined, followed by, if necessary, alcoholysis in the presence of a compound of formula Xl in which R ^xy does not represent hydrogen.

Compounds of formula XVII or XIX may be prepared by reduction of a compound of formula XXV,

wherein W ^x represents W ¹ or W ³ (as appropriate), W represents W ² or W ⁴ (as appropriate), T represents -C(O)- or -CH(OH)- and W ¹ , W ² , W ³ , W ⁴ , X ¹ , X ² , Z ^q1 and Z ^q2 are as hereinbefore defined, under standard reaction conditions known to those skilled in the art, for example reduction in the presence of a suitable reducing reagent such as LiAIH ₄ , NaBH ₄ or trialkylsilane (e.g. triethylsilane) or reduction by hydrogenation (e.g. in the presence of Pd/C).

Alternatively, compounds of formula XVII or XIX may be prepared by reaction of a compound of formula XXVI,

wherein Y represents a suitable group such as -OH, bromo, chloro or iodo, and

W ^x , Z ^q1 and X ¹ are as hereinbefore defined, with a compound of formula XXVIII as defined hereinafter in which M represents hydrogen under standard conditions, for example, such as those described hereinafter in respect of preparation of compounds of formula XXV in which T represents -C(O)- (e.g. in the presence of a Lewis or Brønsted acid). Alternatively, such compounds may be prepared from reaction of a compound of formula XXVI in which Y represents bromo or chloro with a compound corresponding to a compound of formula XXVIII but in which M represents -BF ₃ K (or the like), for example in accordance with the procedures described in Molander et al, J. Org. Chem. 71, 9198 (2006).

Compounds of formula XX may be prepared in several ways. For example, compounds of formula XX in which W ⁵ and/or W ⁶ represent an alkali metal such as lithium, may be prepared from a corresponding compound of formula XVII (in particular those in which Z ^q1 and/or Z ^q2 represents a chloro or sulfonate group or, especially, a protected -NH ₂ group, wherein the protecting group is preferably a lithiation-directing group, e.g. an amido group, such as a pivaloylamido group), by reaction with an organolithium base, such as n-BuLi, S-BuLi, f-BuLi, lithium diisopropylamide or lithium 2,2,6,6-tetramethylpiperidine (which organolithium base is optionally in the presence of a suitable additive, solvent or co-solvent (for example, a lithium co-ordinating agent or a polar aprotic solvent, such as an ether (e.g. dimethoxyethane, tetrahydrofuran or diethyl ether) or an amine (e.g. tetramethylethylenediamine (TMEDA), (-)sparteine or 1,3-dimethyl-3,4,5,6- tetrahydro-2(1H)-pyrimidinone (DMPU)) and the like), at sub-ambient temperatures (e.g. O ⁰ C to -78°C) under an inert atmosphere. Alternatively, such compounds of formula XX may be prepared by reaction of a compound of formula XIX in which W ³ and/or W ⁴ represents chloro, bromo or iodo by a halogen-lithium reaction in the presence of an organolithium base such as t- or π-butyllithium under reaction conditions such as those described above. Compounds of formula XX in which W ⁵ and/or W ⁶ represent -Mg-halide may be prepared from a corresponding compound of formula XIX in which W ³ and/or W ⁴ represents halo

8 000724

39

(e.g. bromo), for example optionally in the presence of a catalyst (e.g. FeCI ₃ ) under standard Grignard conditions known to those skilled in the art. The skilled person will also appreciate that the magnesium of the Grignard reagent or the lithium of the lithiated species may be exchanged to a different metal (i.e. a transmetallation reaction may be performed), for example to form compounds of formula XX in which W ⁵ and/or W ⁶ represent a zinc-based group (e.g. using ZnCI ₂ ).

Compounds of formulae II, Vl, XVI and XXII in which R ^x and R ^y represent hydrogen may be prepared from corresponding compounds of formula I in which R ^x and R ^y do not represent hydrogen under standard hydrolysis conditions, for example such as those described hereinbefore in respect of preparation of compounds of formula I (process (ix) above).

Compounds of formulae II, Vl, XVI and XXII in which R ^x and R ^y do not represent hydrogen may be prepared from corresponding compounds of formula I in which R ^x and R ^y represent hydrogen under standard esterification conditions, for example such as those described hereinbefore in respect of preparation of compounds of formula I (process (x) above) in the presence of an alcohol of formula X as hereinbefore defined.

Compounds of formula XXIIIA, or protected derivatives thereof, may be prepared by reaction of a compound of formula XXVIA,

XXVIA

wherein X ^q represents -OH, -NH ₂ or -N ₃ , and R ^a is as hereinbefore defined, under standard reaction conditions, for example:

(i) when X ^q represents -OH, under Schmidt reaction conditions, or variants thereof, in the presence of HN ₃ (which may be formed in by contacting NaN ₃ with a strong acid such as H ₂ SO ₄ ). Variants include reaction with diphenyl phosphoryl

B2008/000724

40 azide ((PhO) ₂ P(O)N ₃ ) in the presence of an alcohol (such as terf-butanol; thereby forming a f-Boc protected derivative of formula XXVIA) which may result in the formation of a carbamate intermediate;

(ii) when X ^q represents -NH ₂ , under Hoffmann rearrangement reaction conditions, for example in the presence of NaOBr (which may be formed by contacting NaOH and Br ₂ ) which may result in the formation of a carbamate intermediate; (iii) when X ^q represents -N ₃ (which compound itself may be prepared from the corresponding acyl hydrazide under standard diazotization reaction conditions, e.g. in the presence of NaNO ₂ and a strong acid such as H ₂ SO ₄ or HCI) ₁ under Curtius rearrangement reaction conditions, which may result in the formation of an intermediate isocyanate (or a carbamate if treated with an alcohol), all of which may be followed by, if necessary (e.g. if the formation of the free amine is desired), hydrolysis, for example in the presence of water and base (e.g. one hereinbefore described in respect of process step (i) above) when a lower alkyl carbamate (e.g. methyl or ethyl carbamate) is formed as an intermediate or under acidic conditions when e.g. a te/t-butyl carbamate is formed as an intermediate, or, when a benzyl carbamate intermediate is formed, under hydrogenation reaction conditions (e.g. catalytic hydrogenation reaction conditions in the presence of a precious metal catalyst such as Pd).

Alternatively, compounds of formula XXIIIA in which R ^a represents hydrogen, may be prepared by reaction of a compound of formula XXVIB,

XXVIB

wherein X ^a is as hereinbefore defined, under oxidation reaction conditions, for example such as those described in Sheibley, F. E. and McNulty, J. S. J. Org.

Chem., 1956; 21 , 171-173, e.g. in the presence of H ₂ O ₂ , which is preferably in the presence of an alkaline solution.

T/GB2008/000724

41

Compounds of formula XXV in which T represents -C(O)- may be prepared by reaction of a compound of formula XXVII,

XXVII

wherein T ^x represents -C(O)CI or -C=N-NH(f-butyl) (or the like) and W, Z ^q1 and X ¹ are as hereinbefore defined, with a compound of formula XXVIII,

XXVIII

wherein M represents hydrogen or an appropriate alkali metal group (e.g. sodium, potassium or, especially, lithium), a -Mg-halide or a zinc-based group, or, a bromo group, and X ² , Z ^q2 and W are as hereinbefore defined, under reaction conditions known to those skilled in the art. For example in the case of reaction of a compound of formula XXVII in which T represents -C(O)CI with a compound of formula XXVIII in which M represents hydrogen, in the presence of an appropriate Lewis acid. In the case where M represents an appropriate alkali metal group, a -Mg-halide or a zinc-based group, under reaction conditions such as those hereinbefore described in respect of preparation of compounds of formula Il or Vl (process step (IV) above) and preparation of compounds of formula XIII. In the case of a reaction of a compound of formula XXVII in which T represents -C=N-NH(f-butyl) (or the like) with a compound of formula XXVIII in which M represents bromo, under reaction conditions such as those described in Takemiya et al, J. Am. Chem. Soc. 128, 14800 (2006).

For compounds of formula XXV in which T represents -CH(OH)-, reaction of a compound corresponding to a compound of formula XXVII, but in which T represents -C(O)H, with a compound of formula XXVIII as defined above, under

reaction conditions' such as those hereinbefore described in respect of preparation of compounds of formula XXV in which T represents -C(O)-.

Compounds of formula XXIV may be prepared by reaction of a compound of formula XXIX ₁

wherein X ^z represents fluoro or bromo and X ^a is as hereinbefore defined, under standard conditions, for example when X ^z represents fluoro, in the presence of an appropriate source of cyanide ions (e.g. KCN) under standard nucleophilic aromatic substitution reaction conditions or, when X ^z represents bromo, under palladium catalysed cyanation reaction conditions.

Compounds of formula XXVIB may be prepared by reaction of a compound of formula XXX,

wherein X ^a is as hereinbefore defined, with chloral hydrate, hydroxylamine hydrochloride, sodium sulfate and hydrochloric acid, followed by reaction in the presence of concentrated sulfuric acid, for example as described in the Sheibley et a/ journal article referenced herein.

Compounds of formulae III, IV, V, VII, VIII ₁ IX, X, Xl, XII, XIII, XIV, XVIII, XXI, XXVI, XXVIA, XXVII, XXVIII, XXIX and XXX (as well as other compounds, e.g. some compounds of formulae XV, XXIII and XXIV) are either commercially available, are known in the literature, or may be obtained either by analogy with the processes described herein, or by conventional synthetic procedures, in

00724

43 accordance with standard techniques, from available starting materials using appropriate reagents and reaction conditions. In this respect, the skilled person may refer to inter alia "Comprehensive Organic Synthesis" by B. M. Trost and I. Fleming, Pergamon Press, 1991.

The substituents X ¹ , X ² , R ^x , R ^y , R ^w , R ^z Y ¹ and Y ² in final compounds of the invention or relevant intermediates may be modified one or more times, after or during the processes described above by way of methods that are well known to those skilled in the art. Examples of such methods include substitutions, reductions, oxidations, alkylations, acylations, hydrolyses, esterifications, etherifications, halogenations or nitrations. Such reactions may result in the formation of a symmetric or asymmetric final compound of the invention or intermediate. The precursor groups can be changed to a different such group, or to the groups defined in formula I, at any time during the reaction sequence. For example, in cases where R ^x and/or R ^y does not initially represent hydrogen (so providing at least one ester functional group), the skilled person will appreciate that at any stage during the synthesis (e.g. the final step), the relevant R ^x and/or

R ^y -containing group may be hydrolysed to form a carboxylic acid functional group

(i.e. a group in which R ^x and/or R ^y represent hydrogen). In this respect, the skilled person may also refer to "Comprehensive Organic Functional Group

Transformations" by A. R. Katritzky, O. Meth-Cohn and C. W. Rees, Pergamon

Press, 1995.

Compounds of the invention may be isolated from their reaction mixtures using conventional techniques (e.g. recrystallisations).

It will be appreciated by those skilled in the art that, in the processes described above and hereinafter, the functional groups of intermediate compounds may need to be protected by protecting groups.

The protection and deprotection of functional groups may take place before or after a reaction in the above-mentioned schemes.

Protecting groups may be removed in accordance with techniques that are well known to those skilled in the art and as described hereinafter. For example,

protected compounds/intermediates described herein may be converted chemically to unprotected compounds using standard deprotection techniques. By 'protecting group' we also include suitable alternative groups that are precursors to the actual group that it is desired to protect. For example, instead of a 'standard' amino protecting group, a nitro or azido group may be employed to effectively serve as an amino protecting group, which groups may be later converted (having served the purpose of acting as a protecting group) to the amino group, for example under standard reduction conditions described herein.

The type of chemistry involved will dictate the need, and type, of protecting groups as well as the sequence for accomplishing the synthesis.

The use of protecting groups is fully described in "Protective Groups in Organic Synthesis", 3 ^rd edition, T.W. Greene & P. G. M. Wutz, Wiley-lnterscience (1999).

Medical and Pharmaceutical Uses

Compounds of the invention are indicated as pharmaceuticals. According to a further aspect of the invention there is provided a compound of the invention, as hereinbefore defined but without proviso (c), for use as a pharmaceutical.

Although compounds of the invention may possess pharmacological activity as such, certain pharmaceutically-acceptable (e.g. "protected") derivatives of compounds of the invention may exist or be prepared which may not possess such activity, but may be administered parenterally or orally and thereafter be metabolised in the body to form compounds of the invention. Such compounds (which may possess some pharmacological activity, provided that such activity is appreciably lower than that of the "active" compounds to which they are metabolised) may therefore be described as "prodrugs" of compounds of the invention.

By "prodrug of a compound of the invention", we include compounds that form a compound of the invention, in an experimentally-detectable amount, within a predetermined time (e.g. about 1 hour), following oral or parenteral administration. All prodrugs of the compounds of the invention are included within the scope of the invention.

Furthermore, certain compounds of the invention (including, but not limited to, compounds of formula I in which any of R ^x and R ^y are other than hydrogen, so forming an ester group) may possess no or minimal pharmacological activity as such, but may be administered parenterally or orally, and thereafter be metabolised in the body to form compounds of the invention that possess pharmacological activity as such (including, but not limited to, corresponding compounds of formula I, in which R ^x and/or R ^y represent hydrogen). Such compounds (which also includes compounds that may possess some pharmacological activity, but that activity is appreciably lower than that of the

"active" compounds of the invention to which they are metabolised), may also be described as "prodrugs".

Thus, the compounds of the invention are useful because they possess pharmacological activity, and/or are metabolised in the body following oral or parenteral administration to form compounds which possess pharmacological activity.

Compounds of the invention may inhibit leukotriene (LT) C ₄ synthase, for example as may be shown in the test described below, and may thus be useful in the treatment of those conditions in which it is required that the formation of e.g.

LTC ₄ , LTD ₄ or LTE ₄ is inhibited or decreased, or where it is required that the activation of a Cys-LT receptor (e.g. Cys-LTi or CyS-LT ₂ ) is inhibited or attenuated. The compounds of the invention may also inhibit microsomal glutathione S-transferases (MGSTs), such as MGST-I, MGST-II and/or MGST-IlI, thereby inhibiting or decreasing the formation of LTD ₄ , LTE ₄ or, especially, LTC ₄ .

Compounds of the invention may also inhibit the activity of 5-lipoxygenase- activating protein (FLAP), for example as may be shown in a test such as that described in MoI. Pharmacol., 41, 873-879 (1992). Hence, compounds of the invention may also be useful in inhibiting or decreasing the formation of LTB ₄ .

Compounds of the invention are thus expected to be useful in the treatment of disorders that may benefit from inhibition of production (i.e. synthesis and/or

biosynthesis) of leukotrienes (such as LTC ₄ ), for example a respiratory disorder and/or inflammation.

The term "inflammation" will be understood by those skilled in the art to include any condition characterised by a localised or a systemic protective response, which may be elicited by physical trauma, infection, chronic diseases, such as those mentioned hereinbefore, and/or chemical and/or physiological reactions to external stimuli (e.g. as part of an allergic response). Any such response, which may serve to destroy, dilute or sequester both the injurious agent and the injured tissue, may be manifest by, for example, heat, swelling, pain, redness, dilation of blood vessels and/or increased blood flow, invasion of the affected area by white blood cells, loss of function and/or any other symptoms known to be associated with inflammatory conditions.

The term "inflammation" will thus also be understood to include any inflammatory disease, disorder or condition per se, any condition that has an inflammatory component associated with it, and/or any condition characterized by inflammation as a symptom, including inter alia acute, chronic, ulcerative, specific, allergic and necrotic inflammation, and other forms of inflammation known to those skilled in the art. The term thus also includes, for the purposes of this invention, inflammatory pain, pain generally and/or fever.

Where a condition has an inflammatory component associated with it, or a condition characterized by inflammation as a symptom, the skilled person will appreciate that compounds of the invention may be useful in the treatment of the inflammatory symptoms and/or the inflammation associated with the condition.

Accordingly, compounds of the invention may be useful in the treatment of allergic disorders, asthma, childhood wheezing, chronic obstructive pulmonary disease, bronchopulmonary dysplasia, cystic fibrosis, interstitial lung disease (e.g. sarcoidosis, pulmonary fibrosis, scleroderma lung disease, and usual interstitial in pneumonia), ear nose and throat diseases (e.g. rhinitis, nasal polyposis, and otitis media), eye diseases (e.g. conjunctivitis and giant papillary conjunctivitis), skin diseases (e.g. psoriasis, dermatitis, and eczema), rheumatic diseases (e.g. rheumatoid arthritis, arthrosis, psoriasis arthritis, osteoarthritis,

systemic lupus erythematosus, systemic sclerosis), vasculitis (e.g. Henoch- Schonlein purpura, Lδffler ^' s syndrome and Kawasaki disease), cardiovascular diseases (e.g. atherosclerosis), gastrointestinal diseases (e.g. eosinophilic diseases in the gastrointestinal system, inflammatory bowel disease, irritable bowel syndrome, colitis, celiaci and gastric haemorrhagia), urologic diseases (e.g. glomerulo-nephritis, interstitial cystitis, nephritis, nephropathy, nephrotic syndrome, hepatorenal syndrome, and nephrotoxicity), diseases of the central nervous system (e.g. cerebral ischemia, spinal cord injury, migraine, multiple sclerosis, and sleep-disordered breathing), endocrine diseases (e.g. autoimmune thyroiditis, diabetes-related inflammation), urticaria, anaphylaxis, angioedema, oedema in Kwashiorkor, dysmenorrhoea, burn-induced oxidative injury, multiple trauma, pain, toxic oil syndrome, endotoxin chock, sepsis, bacterial infections (e.g. from Helicobacter pylori, Pseudomonas aerugiosa or Shigella dysenteriae), fungal infections (e.g. vulvovaginal candidasis), viral infections (e.g. hepatitis, meningitis, parainfluenza and respiratory syncytial virus), sickle cell anemia, hypereosinofilic syndrome, and malignancies (e.g. Hodgkins lymphoma, leukemia (e.g. eosinophil leukemia and chronic myelogenous leukemia), mastocytos, polycytemi vera, and ovarian carcinoma). In particular, compounds of the invention may be useful in treating allergic disorders, asthma, rhinitis, conjunctivitis, COPD, cystic fibrosis, dermatitis, urticaria, eosinophilic gastrointestinal diseases, inflammatory bowel disease, rheumatoid arthritis, osteoarthritis and pain.

Compounds of the invention are indicated both in the therapeutic and/or prophylactic treatment of the above-mentioned conditions.

According to a further aspect of the present invention, there is provided a method of treatment of a disease which is associated with, and/or which can be modulated by inhibition of, LTC ₄ synthase and/or a method of treatment of a disease in which inhibition of the synthesis of LTC ₄ is desired and/or required (e.g. respiratory disorders and/or inflammation), which method comprises administration of a therapeutically effective amount of a compound of the invention, as hereinbefore defined but without provisos (a) to (c), to a patient suffering from, or susceptible to, such a condition.

8 000724

48 "Patients" include mammalian (including human) patients.

The term "effective amount" refers to an amount of a compound, which confers a therapeutic effect on the treated patient. The effect may be objective (i.e. measurable by some test or marker) or subjective (i.e. the subject gives an indication of or feels an effect).

Compounds of the invention will normally be administered orally, intravenously, subcutaneously, buccally, rectally, dermally, nasally, tracheally, bronchially, sublingually, by any other parenteral route or via inhalation, in a pharmaceutically acceptable dosage form.

Compounds of the invention may be administered alone, but are preferably administered by way of known pharmaceutical formulations, including tablets, capsules or elixirs for oral administration, suppositories for rectal administration, sterile solutions or suspensions for parenteral or intramuscular administration, and the like.

Such formulations may be prepared in accordance with standard and/or accepted pharmaceutical practice.

According to a further aspect of the invention there is thus provided a pharmaceutical formulation including a compound of the invention, as hereinbefore defined but without proviso (c), in admixture with a pharmaceutically acceptable adjuvant, diluent or carrier.

Preferred pharmaceutical formulations include those in which the active ingredient is present in at least 1% (such as at least 10%, preferably in at least 30% and most preferably in at least 50%) by weight. That is, the ratio of active ingredient to the other components (i.e. the addition of adjuvant, diluent and carrier) of the pharmaceutical composition is at least 1 :99 (e.g. at least 10:90, preferably at least 30:70 and most preferably at least 50:50) by weight.

The invention further provides a process for the preparation of a pharmaceutical formulation, as hereinbefore defined, which process comprises bringing into

association a compound of the invention, as hereinbefore defined, or a pharmaceutically acceptable salt thereof with a pharmaceutically-acceptable adjuvant, diluent or carrier.

Compounds of the invention may also be combined with other therapeutic agents that are useful in the treatment of a respiratory disorder (e.g. thromboxane receptor (TP) antagonists or, preferably, leukotriene receptor antagonists (LTRAs), glucocorticoids, antihistamines, beta-adrenergic drugs, anticholinergic drugs and PDE ₄ inhibitors and/or other therapeutic agents that are useful in the treatment of a respiratory disorder) and/or other therapeutic agents that are useful in the treatment of inflammation and disorders with an inflammatory component (e.g. NSAIDs, coxibs, corticosteroids, analgesics, inhibitors of 5- lipoxygenase, inhibitors of FLAP (5-lipoxygenase activating protein), immunosuppressants and sulphasalazine and related compounds and/or other therapeutic agents that are useful in the treatment of inflammation).

According to a further aspect of the invention, there is provided a combination product comprising:

(A) a compound of the invention, as hereinbefore defined but without provisos (a) to (c); and

(B) another therapeutic agent that is useful in the treatment of a respiratory disorder and/or inflammation, wherein each of components (A) and (B) is formulated in admixture with a pharmaceutically-acceptable adjuvant, diluent or carrier.

Such combination products provide for the administration of a compound of the invention in conjunction with the other therapeutic agent, and may thus be presented either as separate formulations, wherein at least one of those formulations comprises a compound of the invention, and at least one comprises the other therapeutic agent, or may be presented (i.e. formulated) as a combined preparation (i.e. presented as a single formulation including a compound of the invention and the other therapeutic agent).

Thus, there is further provided:

(1) a pharmaceutical formulation including a compound of the invention, as hereinbefore defined but without provisos (a) to (c), another therapeutic agent that is useful in the treatment of a respiratory disorder and/or inflammation, and a pharmaceutically-acceptable adjuvant, diluent or carrier; and

(2) a kit of parts comprising components:

(a) a pharmaceutical formulation including a compound of the invention, as hereinbefore defined without provisos (a) to (c), in admixture with a pharmaceutically-acceptable adjuvant, diluent or carrier; and (b) a pharmaceutical formulation including another therapeutic agent that is useful in the treatment of a respiratory disorder and/or inflammation in admixture with a pharmaceutically-acceptable adjuvant, diluent or carrier, which components (a) and (b) are each provided in a form that is suitable for administration in conjunction with the other.

The invention further provides a process for the preparation of a combination product as hereinbefore defined, which process comprises bringing into association a compound of the invention, as hereinbefore defined, or a pharmaceutically acceptable salt thereof with the other therapeutic agent that is useful in the treatment of a respiratory disorder and/or inflammation, and at least one pharmaceutically-acceptable adjuvant, diluent or carrier.

By "bringing into association", we mean that the two components are rendered suitable for administration in conjunction with each other.

Thus, in relation to the process for the preparation of a kit of parts as hereinbefore defined, by bringing the two components "into association with" each other, we include that the two components of the kit of parts may be: (i) provided as separate formulations (i.e. independently of one another), which are subsequently brought together for use in conjunction with each other in combination therapy; or

(ii) packaged and presented together as separate components of a "combination pack" for use in conjunction with each other in combination therapy.

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51

Compounds of the invention may be administered at varying doses. Oral, pulmonary and topical dosages may range from between about 0.01 mg/kg of body weight per day (mg/kg/day) to about 100 mg/kg/day, preferably about 0.01 to about 10 mg/kg/day, and more preferably about 0.1 to about 5.0 mg/kg/day. For e.g. oral administration, the compositions typically contain between about

0.01 mg to about 500 mg, and preferably between about 1 mg to about 100 mg, of the active ingredient. Intravenously, the most preferred doses will range from about 0.001 to about 10 mg/kg/hour during constant rate infusion.

Advantageously, compounds may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three or four times daily.

In any event, the physician, or the skilled person, will be able to determine the actual dosage which will be most suitable for an individual patient, which is likely to vary with the route of administration, the type and severity of the condition that is to be treated, as well as the species, age, weight, sex, renal function, hepatic function and response of the particular patient to be treated. The above- mentioned dosages are exemplary of the average case; there can, of course, be individual instances where higher or lower dosage ranges are merited, and such are within the scope of this invention.

Compounds of the invention may have the advantage that they are effective inhibitors of LTC ₄ synthase.

Compounds of the invention may also have the advantage that they may be more efficacious than, be less toxic than, be longer acting than, be more potent than, produce fewer side effects than, be more easily absorbed than, and/or have a better pharmacokinetic profile (e.g. higher oral bioavailability and/or lower clearance) than, and/or have other useful pharmacological, physical, or chemical properties over, compounds known in the prior art, whether for use in the above- stated indications or otherwise.

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52 Biological Test

In the assay LTC ₄ synthase catalyses the reaction where the substrate LTA ₄ methyl ester is converted to LTC ₄ methyl ester. Recombinant human LTC ₄ synthase is expressed in Piccia pastoralis and the purified enzyme is dissolved in

25 mM Tris-buffer pH 7.8 and stored at -20 ⁰ C. The assay is performed in phosphate buffered saline (PBS) pH 7.4, supplemented with 5 mM glutathione

(GSH). The reaction is terminated by addition of acetonitrile / MeOH / acetic acid

(50/50/1 ). The assay is performed at rt in 96-well plates. Analysis of the formed LTC ₄ methyl ester is performed with reversed phase HPLC (Waters 2795 utilizing an Onyx Monolithic C18 column). The mobile phase consists of acetonitrile /

MeOH / H ₂ O (32.5/30/37.5) with 1% acetic acid pH adjusted with NH ₃ to pH 5.6, and absorbance measured at 280 nm with a Waters 2487 UV-detector.

The following is added chronologically to each well:

1. 50 μl assay buffer, PBS with 5mM GSH.

2. 0.5 μl inhibitor in DMSO.

3. 2 μl LTC ₄ synthase in PBS. The total protein concentration in this solution is 0.025 mg/ml. Incubation of the plate at room temperature for 10 minutes.

4. 0.5 μl LTA ₄ methyl ester. Incubation of the plate at rt for 1 min.

5. 50 μl stop solution.

80 μl of the incubation mixture is analysed with HPLC.

Examples

The invention is illustrated by way of the following examples, in which the following abbreviations may be employed:

BINAP 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl

DMF dimethylformamide

EtOAc ethyl acetate

MeOH methanol

NMR nuclear magnetic resonance rt room temperature

B2008/000724

53 rx reflux

THF tetrahydrofuran

Chemicals specified in the synthesis of the compounds in the examples were commercially available from, e.g. Sigma-AIdrich Fine Chemicals, Maybridge or Acros Organics.

Starting materials I-V:

5,5'-Methylenebis(salicylic acid) (4,4'-dihvdroxydiphenylmethane-3,3'-dicarboxylic acid; CAS number: 122-25-8) (I)

The starting material 5,5'-methylenebis(salicylic acid) (I) is commercially available (from e.g. Acros Organics).

Preparation of dimethyl 5,5'-methylenebis(2-hydroxybenzoate) (II):

Concentrated H ₂ SO ₄ (2 ml.) was added dropwise to a stirred suspension of I (7.2 g) in MeOH (20 ml.) at rt. After stirring at rx for 10 h, the mixture was allowed to cool to rt before EtOAc (20 mL) was added. The mixture was washed with NaHCO ₃ (aq, sat) until the washings turned weakly basic. The organic phase was dried (Na ₂ SO ₄ ), concentrated and purified by chromatography, providing the title compound (II) in 1.3 g (16.4%) yield.

Preparation of dimethyl 5,5'-methylenebis(2-(trifluoromethylsulfonyloxy)- benzoate) (III):

A suspension of Il (0.79 g, 2.50 mmol) in toluene (10 mL) was mixed with K ₃ PO ₄ (aq, 3 g in 10 mL water), cooled to 0 ⁰ C, before triflic anhydride (1.7 g, 6.0 mmol) was added dropwise whilst stirring vigorously and maintaining the reaction temperature below 10 ⁰ C. The mixture was stirred 2 h at rt, the layers were separated and the organic phase washed with water and concentrated. The residue was purified by chromatography, affording the title compound (III) in 0.786 g (54%) yield.

008/000724

54 Preparation of dimethyl 5,5'-methylenebis(2-aminobenzoate) (IV):

To a stirred solution of 60.5 g methyl 2-aminobenzoate, HCI (aq, sat, 144 ml_) and water (500 mL) was slowly added formaldehyde (aq, 3%, 155 ml_) at 50 ⁰ C over a period of 20 mins. The solution was heated with stirring at 80 ⁰ C for 6 h. After cooling to room temperature, the solution was neutralised with ammonia and a precipitation was formed which was filtered off, washed with water, dried and recrystalized from EtOH to give the product (IV) as a yellowish powder in 42.1 g (86%).

Preparation of 5,5'-methylenebis(2-amino-3-chlorobenzoic acid) (V):

To a stirred mixture of 2-amino-3-chlorobenzoic acid (1.06 g, 6.20 mmol), water (20 mL), and HCI (aq, 37%, 4 mL) at 50 ⁰ C was added 3% aqueous formaldehyde (93.10 mg, 3.10 mmol). The mixture was heated at 70 ⁰ C and stirred for 4 h. After cooling, the white precipitate was filtered off, washed with water and MeOH to afford the title compound (952 mg, 86 %) as a white solid. ¹ H NMR (DMSO-Cf ₆ , 400 MHz), δ 7.59-7.55 (2H, m), 7.38-7.34 (2H, m), 3.69 (2H, s). ¹³ C δ 168.6, 144.9, 133.8, 129.9, 127.9, 118.8, 111.4, 37.8.

5,5'-methylenebis(2-aminobenzoic acid) (Vl) (which is commercially available from e.g. Maybridge or, alternatively, may be prepared as described in the literature, e.g. Bioorg.. Med. Chem., 2006, 14, 2209) may be esterified under standard conditions known to those skilled in the art (which may involve the use of protecting groups) in order to give dimethyl 5,5'-methylenebis(2- aminobenzoate) (IV).

General Methods Producing Exemplified Compounds 1-47

General method A for diarylamine coupling of IH to produce dimethyl 5,5'-methylenebis(2-(arylamino)benzoate) VH. followed by hydrolysis to produce 5,5'-methylenebis(2-(arylamino)benzoic acid) VIII:

A mixture of compound III (0.196 g, 1 equiv), arylamine (1.2 equiv), Cs ₂ CO ₃ (308 mg, 1.4 equiv), Pd(OAc) ₂ (7.6 mg, 0.05 equiv), and BINAP (32 mg, 0.075 equiv)

in toluene (1.34 mL) was stirred at 100 ⁰ C for 10 h. The mixture was filtered, concentrated and the residue purified by chromatography to furnish compound VII (see the yield of the 'ester' in Table 1 ). A mixture of VII (1 equiv), NaOH (aq, 2M, 2.8 mL) and dioxane (5.6 mL) was stirred for 5 h at 120 ⁰ C, cooled to rt, acidified with HCI (aq, 10%, pH ~ 2-5), and extracted with EtOAc. The combined extracts were dried (Na ₂ SO ₄ ) and concentrated to furnish compound VIII (see the yield of the acid in Table 1 ).

General method B for diarylamine coupling of IV to produce dimethyl 5,5'-methylenebis(2-(arylamino)benzoate) VII. followed by hydrolysis to produce 5,5'-methylenebis(2-(arylamino)benzoic acid) VIII:

An oven-dried vessel was charged with compound IV (0.157 g, 0.5 mmol), arylboronic acid (2 mmol), Cu(OAc) ₂ (184 mg, 1 mmol), pyridine (82 μL, 1 mmol), triethylamine (140 μL, 1 mmol), dichloromethane (15 mL) and 4 A molecular sieves. The mixture was stirred at rt for 4 days, filtered through Celite ^® and purified by chromatography, furnishing di- and mono-arylated compounds. Subsequent hydrolysis was carried out in accordance with the procedure described in Method A.

General method C for diarylamine coupling of IV to produce dimethyl 5,5'-methylenebis(2-(arylamino)benzoate) VII, followed by hydrolysis to produce 5,5'-methylenebis(2-(arylamino)benzoic acid) VIII:

A mixture of compound IV (0.314 g, 1 mmol), copper(l)tris(triphenyl- phosphine)bromide (372 mg, 0.4 mmol), Cs ₂ CO ₃ (977 mg, 3 mmol), and toluene (15 mL) was heated under argon at 110 ⁰ C for 5 min. The aryl iodide (2 mmol) was added via syringe and the mixture was stirred at 110 ⁰ C for 1-2 days. After cooling, the mixture was filtered through a small pad of silica gel, concentrated and purified by chromatography, furnishing the di-arylated compound as the minor product and the mono-arylated as the major product. The subsequent hydrolysis was carried out in accordance with the procedure described in Method A.

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56

General method D for diarylamine coupling of IV to produce dimethyl 5,5'-methylenebis(2-(arylamino)benzoate) VII. followed by hydrolysis to produce 5.5'-methylenebis(2-(arylamino)benzoic acid) VIII .

An oven-dried vessel was charged with compound IV (0.314 g, 1.0 mmol), Pd ₂ (dba) ₃ (23 mg, 0.025 mmol), Cs ₂ CO ₃ (0.762 g, 2.34 mmol), (rac)-BINAP (23.4 mg, 0.037 mmol), aryl bromide (1.67 mmol) and toluene (3 mL) under argon atmosphere. The mixture was heated at 100 ⁰ C for 2-4 days. If needed, a second addition of the reactants, except compound IV ₁ was made in order to increase the conversion. The mixture was cooled, filtered, and purified by chromatography, furnishing di- and mono-arylated compounds. Subsequent hydrolysis was carried out in accordance with the procedure described in Method A.

General method E for di-alkylation of VII to produce dimethyl 5,5'-methylenebis(2- (aryl(alkyl)amino)benzoate) IX. followed by hydrolysis to produce 5.5'-methylenebis(2-(aryl(alkyl)amino)benzoic acid) X.

Compound VII (0.18 mmol) was added to a mixture of NaH (24 mg, 0.8 mmol, 80% in mineral oil) and DMF (2 mL). The mixture was stirred at rt for 20 min. Alkyl halide (0.8 mmol) was added and the mixture was stirred at rt for 24 h. The mixture was diluted with water (12 mL) and acidified to ~pH 6 with HCI (aq, 1M). Extractive work-up (water, EtOAc) and purification by chromatography gave the desired compounds IX. Subsequent hydrolysis was carried out in accordance with the procedure described in Method A. Purification by chromatography furnished compounds X.

General method F for mono-alkylation of VM to produce 2-falkyl-(aryl)-amino1-5-[4- (arylamino)-3-methoxycarbonyl-benzvn-benzoic acid methyl ester Xl. followed by hydrolysis to produce 2-[alkyl-(aryl)-aminol-5-[3-carboxy-4-(arylamino)-benzyl]- benzoic acid XII.

To a stirred solution of VII (0.63 g, 1.2 mmol) in DMF (60 ml), n-butyl iodide (0.40 mL, 3.5 mmol) and NaH (47 mg, 1.2 mmol, 60% suspension in mineral oil) were added and the reaction mixture was stirred at room temperature for 1 h. The addition of water followed by an extractive workup (EtOAc, water, brine) and

purification by chromatography gave the desired compounds Xl (see the yield of the ester given in Table 1 ). A mixture of Xl (0.58 g, 0.97 mmol), NaOH (0.28 g, 6.9 mmol), MeOH (25 mL) and water (2 mL) was stirred for 3 h at reflux, cooled to rt, concentrated in vacuo, diluted with brine (20 mL) acidified with HCI (1 M, pH -2-5), and extracted with EtOAc. The combined extracts were dried (Na ₂ SO ₄ ), concentrated and purified by column chromatography to furnish compound XII (see the yield of the acid in Table 1 ).

Table 1. Compounds of Examples 1-42 using general Method A-F

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61

^* Pd(OAc) ₂ was used as the palladium source (5 mol-%)

^# Hydrolyzed according to the procedure in General Method F.

Table 2. Spectroscopic data of the compounds of Examples 1-42

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General Procedure for Preparation of Unsymmetrical Diaryl-substituted Compounds

Mono-arylated ester compounds were synthesised in accordance with Method C. The second arylation step was performed in accordance with Method B to furnish the desired unsymmetrical diaryl-substituted compounds, which compounds were then subjected to hydrolysis.

Table 3. Unsymmetrical Diaryl-substituted Compounds of Examples 43-47 using general Method C followed by general Method B

* Mono-arylated ester compound was synthesized in accordance with Method B.

Table 4. Spectroscopic data of the compounds of Examples 43-47

General Methods Producing Exemplified Compounds 48-66

General method G for the preparation of Examples 48-58, 61-64:

A mixture of 5,5'-methylenebis(2-aminobenzoic acid) (Vl) (250 mg, 0.873 mmol), arylisocyanate (2.10 mmol), and THF (20 ml_) was stirred at rt overnight. The precipitate was collected (precipitation with n-hexane if necessary) and recrystallised from THF/n-hexane to give the title product as a solid.

24

68 General method H for monocarbamidation for the preparation of Examples 59-60:

A mixture of Vl (250 mg, 0.873 mmol), arylisocyanate (0.291 mmol), and THF (20 mL) (or dioxane (40 mL) in Examples 11-12) was stirred at rt overnight. The product was precipitated with /i-hexane and washed with HCI (aq) to give the title compound as a solid after recrystallisation from MeOH or dioxane/water.

General method I for the preparation of Examples 65-66:

A mixture of V (100 mg, 0.282 mmol), arylisocyanate (0.676 mmol), Et ₃ N (77 mg, 0.762 mmol) and THF (10 mL) was stirred at rt overnight. The precipitate was collected and sonicated with HCI (aq., 2M). The solid was filtered off, washed with HCI (aq., 2M), water and THF to afford the title product as a solid.

Table 5. Compounds of Examples 48-66

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Table 6 Physical properties of the compounds of Examples 48-66

- ¹ H NMR (DMSO-Of ₆ , 400 MHz), δ

Example

No.

¹³ C NMR (DMSO-Qf ₆ , 100 MHz), δ

¹ H; 13.42 (2H, br s), 10.31 (2H, s), 9.96 (2H, s), 8.28 (2H d), 7 85-7.76

(2H m), 7.74-7.72 (2H, m), 7.48-7.42 (2H, m), 7.39-7-34 (2H , m), 7.29

(2H t), 7.04-6.98 (2H, m), 3.93 (2H, s).

48

¹³ C; 169.2, 152.0, 141.3, 140.0, 134.1, 133.8, 133.0, 130 6 130.2,

121 5, 120.2, 117.8, 116.8, 115.7, 38.9.

H; 13.36 (2H, br s), 10.22 (2H, s), 9.73 (2H, s), 8.28 (2H d), 7. 82-7.77

(2H m), 7.53-7.46 (4H, m), 7.44-7.39 (2H, m), 7.27 (4H ■ t), 6. 97 (2H,

), 3 .92 (2H, s). ¹³ C; 168.9, 152.0, 140.1, 139.5, 133.8, 133 4 , 130.4,

128 4 121.8,120.0, 118.5, 115.4, 38.9.

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¹ H; 13.16 (2H, br s), 9.98 (2H, s), 9.25 (2H, s), 8.07 (2H ■ d), 7.99-7.92

(2H , m), 7.74-7.69 (2H, m), 7.41-7.32 (6H, m), 7.15-7.06 (4H, m),

64 7.05-6.98 (6H, m) , 6 .87- 6.81 (2H, m), 3.90 (2H, s). ¹³ C; 168 .3, 156.6,

152 .5, 147.0, 139 .2, 133.8, 130.5, 130.4, 129.9, 129.4, 123.6, 123.5,

123 .4, 122.7, 121 4, 118.5, 118.2, 117.1, 38.9.

¹ H; 13.21 (2H, br s), 9.93 (2H, s), 8.75 (2H, br s), 8.22-8.15 (4H, m),

65 7.71-7.65 (8H, m). 4.05 (2H, s). ¹³ C; 166.9, 151.7, 146.0, 140 .8, 138.6,

132 4, 132.1 , 130. 1 , 129.4, 128.8, 124.9, 117.1 , 38.3.

H; 13.15 (2H, br s) , 9.40 (2H ₁ s), 8.52 (2H, s), 7.73-7.64 (6H, m),

7.33-7.19 (4H ₁ m) 7 04-6.80 (2H, m), 4.03 (2H, s). ¹³ C; 167. O, 151.9,

O RDR

40 9, 138.2, 132 9, 132.4, 132.3, 130.2, 129.7, 129.0, 128. 7, 121.3,

17. 1, 116.2, 38.2

General methods producing exemplified compounds 67-97

General method for the preparation of Examples 67-81 and 83-85

Intermediate Vl (250 mg, 0.873 mmol) was added in portions to a 50 ⁰ C warm solution of sodium carbonate (466 mg, 2.18 mmol, in 5 ml_ of water). Arylsulfonyl chloride (2.18 mmol) was added to the solution in portions and the resulting mixture was stirred at 70 ^C C for 30 min and then at 85 ^C C for additional 30 min. After cooling to room temperature the reaction mixture was acidified with dilute HCI, the product was collected and washed with dilute HCI and then water to give the title compound as a solid. Recrystallization form an appropriate solvent furnished pure compounds of the Examples as depicted in Table 7.

Method for preparation of Example 82

The compound of Example 81 (0.13 g, 0.2 mmol; see below) was dissolved in CH ₂ CI ₂ (10 mL) and MeOH (1 ml_) and Pd/C (0.045 g, 10%) was added. The mixture was set under hydrogen atmosphere and stirred at rt for 1.5h. Filtration and concentration afforded the crude product which was purified by

recrystallization in ethanol/water to furnish the pure title compound in 85 mg (72%) yield.

Table 7. Compounds of Examples 67-85

Table 8. Physical properties of the compounds of Examples 67-85

¹ H NMR (DMSO-de, 400 MHz), δ No

¹³ C NMR (DMSO-Cf ₆ , 100 MHz), δ

¹ H; 10.95 (2H, br s) 9.67 (2H, s) 8.07 (2H, d, J= 8.6 Hz) 7.82-7.81 (2H, m),

7.73-7.70 (4H, m) 7.43-7.34 (4H ₁ m) 3.88 (2H, s) 2.14 (6H, s). ¹³ C; 169.2,

67

169.0, 139.4, 137.3, 136.0, 134.5, 131.2, 127.7, 126.1, 124.7, 124.4,

119.3, 117.6, 38.5, 23.6.

¹ H; 8.32 (4H, m) 8.02 (4H, m) 7.69-7.67 (2H, m) 7.37-7.28 (4H, m) 3.84

68 (2H, s). ¹³ C; 168.9, 149.6, 145.1, 138.1 , 135.5, 134.1 , 131.1, 128.1, 124.4, 119.4, 118.7, 38.6.

¹ H; 11.32 (2H ₁ br s) 8.24-8.19 (2H, m) 8.20-7.19 (2H, m) 7.90-7.82 (4H ₁ m)

69 7.74-7.72 (2H ₁ m) 7.42-7.33 (4H ₁ m) 3.86 (2H ₁ s). ¹³ C; 169.2, 137.1 , 136.6, 135.4, 134.6, 134.0, 133.2, 131.4, 131.2, 128.8, 128.7, 117.6, 116.2, 38.4. i u H;. 11.04 (2H ₁ br s) 8.05-8.00 (4H, m) 7.98-7.92 (4H ₁ m) 7.71-7.68 (2H, m)

70

133.3, 131.1, 127.4, 119.7, 118.1 , 117.2, 115.6, 38.5.

¹ H; 10.95 (2H ₁ s) 8.28-8.23 (2H, m) 8.18-8.10 (2H, m) 7.98-7.93 (2H, m) 7.69-7.61 (4H, m) 7.43-7.33 (4H, m) 3.86 (2Hr s). ¹³ C; 169.0, 165.4, 138.9, 1 137.0, 136.1, 134.5, 133.7, 131.8, 131.1, 130.5, 129.9, 127.0, 119.5, 117.7, 38.5.

¹ H; 11.67 (2H ₁ br s) 8.31-8.24 (4H ₁ m) 8.06-8.01 (2H ₁ m) 7.75-7.73 (2H, m) 2 7.33-7.28 (4H, m) 3.84 (2H, s). ¹³ C; 169.2, 139.6, 136.5, 135.6, 135.3, 134.7, 132.1, 131.7, 131.3, 131.1 , 117.3, 117.2, 116.5, 116.0, 38.3.

¹ H; 7.93-7.88 (4H ₁ m) 7.72-7.69 (2H ₁ m) 7.54-7.48 (4H ₁ m) 7.41-7.32 (4H, 3 m) 3.86 (2H ₁ s). ¹³ C; 169.0, 151.0, 137.6, 137.5, 135.7, 134.3, 131.1 , 129.3, 121.2, 119.0, 117.7, 38.5.

¹ H; 10.79 (2H ₁ br s) 8.45-8.40 (2H, m) 8.23-8.20 (4H ₁ m) 7.70-7.68 (2H ₁ m) ⁴ 7.39-7.34 (4H ₁ m) 3.91 (2H, s).

¹ H; 10.85 (2H ₁ s) 10.32 (2H ₁ s) 7.74-7.67 (10H ₁ m) 7.42-7.31 (4H ₁ m) 3.8.

75 (2H s) 2.06 (6H, s). "C; 169.2, 168.8, 143.4, 137.8, 135.4, 134.5, 131.7 131.0, 127.9, 118.6, 118.4, 116.6, 38.5, 24.0.

¹ H; 7.68-7.62 (6H, m), 7.40-7.25 (8H, m) 3.80 (2H, s) 2.63-2.55 (4H, m 1.55-1.45 (4H, m) 1.30-1.18 (4H, m) 0.84 (6H ₁ t, J= 7.4 Hz). ¹³ C; 169.2

76 148.0, 138.4, 135.1, 133.9, 130.9, 128.9, 127.1, 126.5, 125.2, 118.3, 38.6, 34.4, 32.4, 21.6, 13.6.

1 H|_|;. 10.99 (2H, br s), 7.97-7.94 (2H, m) 7.82-7.78 (2H, m) 7.74-7.68 (4H ₁ m) 7

134.3, 132.1, 131.5, 131.1 , 128.4, 126.6, 120.0, 118.4, 38.6.

¹ H; 3.67 (S ₁ 6H) 3.78 (s, 6H) 3.86 (s, 2H) 7.04 (d, J=8.5 Hz ₁ 2H) 7.15 (d, 8 J=2.1 Hz ₁ 2H) 7.31-7.50 (m, 6H) 7.71 (d, J=1.8 Hz, 2H) 10.75-10.85 (br s, 2H)

¹ H; 3.76 (S ₁ 2H) 7.27 (d, J=8.6 Hz, 2H) 7.44 (d, J=8.6 Hz, 2H) 7.57-7.77 (m, 9 8H) 7.93-8.17 (m, 6H) 8.52 (s, 2H) 10.8-11.2 (br s, 2H)

¹ H; 3.86 (s, 2H) 7.29-7.40 (m, 4H); 7.66-7.76 (m, 4H); 7.85 (dd, J=8.4 and 0 2.1 Hz, 2H); 8.13 (d, J=2.1 Hz ₁ 2H)

¹ H; 3.85 (S ₁ 2H) 7.35 (dd, J=8.6 and 1.8 Hz, 2H) 7.47 (d, J=8.6 Hz, 2H) 1 7.69-7.91 (m, 6H) 7.99 (dd, J=7.6 and 1.3 Hz, 2H) 8.11 (dd, J=7.4 and 1.5 Hz, 2H) 11.3-11.6 (br s, 2H)

¹ H; 3.81 (S ₁ 2H) 5.8-6.2 (br s, 4H) 6.51-6.62 (m, 2H) 6.78 (d, J=8.2 Hz ₁ 2H) 2 7.18-7.36 (m, 6H) 7.53 (d, J=8.2 Hz ₁ 2H) 7.89 (s, 2H) 11.0-11.6 (br s, 2H)

¹ H; 0.93 (t, J= 7.3 Hz, 6H) 1.35-1.50 (m, 4H) 1.65-1.80 (m, 4H) 3.81 (s, 2H) 3 3.90-3.97 (m, 4H) 6.80-6.91 (m, 4H) 7.20-7.24 (m, 2H) 7.56-7.61 (m, 2H) 7.66-7.71 (m, 2H) 7.72-7.79 (m, 4H) 10.27 (s, 2H)

1| H_|. 4 ; 8.64-8.54 (2H ₁ m) 7.58-7.20 (14H, m) 3.81 (2H, s)

¹ H; 3.87 (S ₁ 2H) 7.33-7.44 (m, 8H) 7.68-7.71 (m, 2H) 7.81-7.88 (m, 4H) 11.0 (br s, 2H)

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Method for benzylation furnishing Examples 86-95

Compound IV (160 mg, 0.5 mmol) was dissolved in an appropriate solvent (acetonitrile, dichloromethane or ethanol). Benzaldehyde (2 mmol) and NaBH(OAc) ₃ (850 mg, 4 mmol) were added and the resulting mixture was stirred at rt for 40-6Oh. Extractive workup (CH ₂ CI ₂ , water), drying (Na ₂ SO ₄ ) of the combined organic extracts and concentration furnished the crude which was purified by chromatography and then hydrolyzed according to general method (e.g. as described in general method A) to give the pure compounds as depicted in Table 9.

Table 9. Compounds of Examples 86-95

Table 10. Physical properties of the compounds of Examples 86-95

No ¹ H NMR (DMSO-Cf ₆ , 400 MHz), δ

7.60 (2H ₁ d, J=2.1 Hz) 7.41-7.29 (4H, m) 7.21-7.07 (6H, m) 6.60 (2H, d,

86 J=8.7 Hz) 4.40 (4H, s) 3.64 (2H, s)

7.69-7.50 (10H, m) 7.12 (2H, dd, J=8.7 and 2.1 Hz) 6.55 (2H, d, J=8.7 Hz)

87 4.54 (4H, s) 3.64 (2H, s)

7.60 (2H, d, J=2.0 Hz) 7.30-7.20 (4H, m) 7.13 (2H ₁ dd, J=8.67 and 2.0 Hz)

88 6.94-9.83 (4H, m) 6.62 (2H ₁ d, J=8.7 Hz) 4.30 (4H, s) 3.72 (6H, s) 3.64 (2H, s)

7.59 (2H, d, J=2.1 Hz) 7.24-7.07 (10H, m) 6.59 (2H ₁ d, J=8.7 Hz) 4.35 (4H,

89 s) 3.64 (2H ₁ S) 2.26 (6H ₁ s)

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7.60 (2H, d, 7=2.1 Hz) 7.42-7.28 (8H, m) 7.12 (2H, dd, 7=8.7 and 2.1 Hz)

90 6.54 (2H, d, 7=8.7 Hz) 4.43 (4H ₁ s) 3.63 (2H, s)

7.60 (2H ₁ d, 7=2.1 Hz) 7.38-7.18 (10H ₁ m) 7.12 (2H ₁ dd, 7=8.6 and 2.1 Hz)

91 6.59 (2H ₁ d, J=8.6 Hz) 4.44 (4H, s) 3.63 (2H ₁ s)

7.59 (2H ₁ d, 7=2.0 Hz) 7.48-7.20 (14H ₁ m) 7.13 (2H ₁ dd, 7=8.6 and 2.0 Hz)

92 7.01-6.92 (4H ₁ m) 6.62 (2H, d, J=8.6 Hz) 5.06 (4H ₁ s) 4.32 (4H, s) 3.64 (2H ₁ s)

7.66 (2H, d, 7=2.0 Hz) 7.42-7.12 (12H ₁ m) 7.07 (2H, dd, 7=8.6 and 2.0 Hz)

93 6.97-6.78 (6H ₁ m) 6.56 (2H ₁ d, 7=8.6 Hz) 5.06 (4H, s) 4.42 (4H ₁ s) 3.64 (2H ₁ s)

8.4-8.1 (2H, br s) 7.63 (2H, d, 7=1.5 Hz) 7.53 (2H, dd, 7=6.7 and 2.7 Hz)

94 7.35-7.23 (4H, m) 7.13 (2H, dd, 7=8.5 and 1.5 Hz) 6.47 (2H, d, 7=8.5 Hz) 4.54 (4H ₁ S) 3.65 (2H, s)

8.7-7.8 (2H, br s) 7.62 (2H ₁ d, 7=1.9 Hz) 7.48-7.42 (2H, m) 7.34 (4H ₁ d,

95 7=1.6 Hz) 7.13 (2H ₁ dd, 7=8.6 and 1.9 Hz) 6.52 (2H, d, 7=8.6 Hz) 4.47 (4H, s) 3.65 (2H, s)

Method for the preparation of Examples 96 and 97

Step 1: To a solution of intermediate Vl (523 mg, 1.83 mmol) in THF was added 4-nitrobenzeneisocyanate (100 mg, 0.610 mmol) and the resulting solution stirred at room temperature overnight. π-Hexane was added, the precipitated product was collected and washed with diluted HCI (aq) to give 2-amino-5-(3-carboxy-4- (3-(4-nitrophenyl)ureido)benzyl)benzoic acid (Example 60 above) as a yellow solid (185 mg, 67%).

Step 2: The foregoing compound of Example 60 (250 mg, 0.555 mmol) was treated with arylsulfonyl chloride (0.666 mmol) and sodium carbonate (235 mg, 2.22 mmol, in 5 ml_ of water) as described above. The crude product was purified by chromatography to give the pure compounds described in Table 11.

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Table 11. Compounds of Examples 96-97

Table 12. Physical properties of the compounds of Examples 96-97

¹ H NMR (DMSO-Cf ₆ , 400 MHz), δ

No ¹³ C NMR (DMSO-Cf ₆ , 100 MHz), δ

¹ H 10.48 (1H, s) 10.43 (1H, s) 8.29-8.24(1 H, m) 8.22-8.16 (2H, m) 7.99-7.97 (1 H, m), 7.85-7.69 (6H, m) 7.47-7.38 (3H, m) 3.93 (2H, s).

96

¹³ C 168.9, 151.5, 146.2, 140.9, 139.4, 136.8, 136.2, 134.3, 133.9, 133.7, 132.1, 131.6, 131.0, 130.6, 128.4, 126.6, 124.8, 120.2, 120.0, 118.5, 117.6, 115.9, 38.7.

¹ H 10.48 (1H, s) 10.42 (1H, s) 8.36-8.31 (2H, m) 8.27-8.23 (1 H, m) 8.22-8.17 (2H ₁ m) 8.07-8.02 (2H ₁ m) 7.79-7.72 (4H ₁ m) 7.42-7.39 (3H, m) 3.91 (2H, s).

97 ¹³ C 168.9, 151.5, 149.7, 146.2, 140.9, 139.4, 136.6, 134.3, 134.0, 133.7, 131.1, 130.6, 128.2, 124.8, 124.5, 120.2, 119.6, 117.6, 115.9, 38.7.

Example 98 Title compounds of the examples were tested in the biological test described above and were found to exhibit 50% inhibition of LTC ₄ at a concentration of 10 μM or below. For example, the following representative compounds of the examples exhibited the following IC ₅₀ values.

Example 6: 5700 nM Example 8: 74O nM

Example 9: 3400 nM

Example 12: 280O nM

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Example 27: 641O nM Example 55: 180O nM Example 57: 4000 nM Example 58: 870 nM Example 59: 4300 nM Example 62: 5800 nM Example 67: 2800 nM Example 69: 130O nM Example 74: 700 nM Example 89: 340O nM Example 93: 2300 nM